Paralysis of the tongue muscles. Damage to the hypoglossal nerve (neuropathy of the hypoglossal nerve, neuropathy of the hypoglossal nerve). What is paralysis

Photo 1. Paralysis significantly impairs quality of life. Source: Flickr (Sven _Dota2).

What is paralysis in medicine

Paralysis (or plegia) is a condition that results from pathological changes in the body. Such processes lead to disruption of motor functions, as a result of which they are completely lost. In most cases, this is not an independent disorder that occurs in isolation. The cause of plegia is always another pathology or a number of diseases.

Forms of paralysis

Paralysis is classified according to several criteria: degree of manifestation, persistence of the process and localization. Pathology can also be divided into forms, which are determined by the degree of damage to the central motor neurons (they are responsible for the possibility of communication between the central nervous system and other cells).

Note! If disturbances occur in the corticospinal tract, central paralysis is diagnosed. When a peripheral motor neuron is affected, paralysis is defined as flaccid or peripheral.

Independent forms of paralysis are considered:

  1. Bell's palsy. In this condition, the facial region is affected and the pathology may be bulbar or pseudobulbar. Bulbar palsy (acute or progressive) is a type of polio and is characterized by atrophy and lack of mobility of the muscles of the larynx and tongue. With pseudobulbar palsy, the facial muscles may lose mobility, but the tongue and larynx are not affected.
  2. Paralysis caused by damage to the brachial plexus. Although this is an acquired disease, it occurs during childbirth. This disorder is known as “obstetric paralysis” and is essentially a type of birth injuries.

There is another independent form - familial myoplegia. In such cases, paralysis is periodic and affects only the limbs. It is believed that this is a hereditary disease that is transmitted in a dominant manner, but the genetics of the pathology of this species is currently not well studied.

Photo 2. The human skeleton is not injured during paralysis; lack of coordination occurs due to impaired muscle mobility. Source: Flickr (Athene Donald)

Localization

Paralysis is also classified by location and can occur either on the same side as the lesion in the central nervous system (ipsilateral) or on the opposite side (collateral).

Additionally, designations are used that characterize the sides and the number of limbs affected by the pathology:

  1. Tetraplegia. The patient is paralyzed in all limbs.
  2. Paraplegia. Paralysis affects only both lower or both upper limbs.
  3. Monoplegia. One of the limbs is paralyzed.

By localization, it is often possible to determine organic disorders of the central nervous system, since paralysis speaks specifically about defects in it.

Causes of paralysis

There are a number of reasons and predisposing factors that lead to the development of paralysis:

  • injuries;
  • infectious diseases;
  • chemical poisoning of the body (for example, lead);
  • disorders in the metabolic system;
  • oncological neoplasms;
  • congenital or acquired diseases of the central nervous system;
  • polyneuritis of alcoholic origin (disease of the nerve trunks);
  • cerebral palsy.

This is interesting! In the history of medicine, a number of cases have been recorded when paralysis occurred in mentally unbalanced people as a result of severe hysterics. In such cases, the central nervous system simply could not stand it and failed, leaving the person unable to move.

Symptoms and signs of pathology

With paralysis, the patient experiences impaired vascular tone, sensory and trophic disorders, impaired sensitivity of the affected organs, possible convulsive tension of the muscles affected by paralysis; with central paralysis, spasmodic contractions are possible.

With paralysis, abdominal reflexes are completely absent or greatly reduced. When the lower extremities are paralyzed, the big toe bends upward when external stimuli act on the patient's foot (Babinski reflex).

Complications

Paralysis itself is a complication that occurs as a result of the development of other pathologies. But independent forms can lead to more severe consequences. Thus, Bell's palsy sometimes causes bilateral damage. facial nerve, and the consequences are irreversible.

With bulbar palsy, asphyxia may develop, which may not occur for years, but may occur already in the first days of the patient’s lesion. If bulbar palsy progresses, the prognosis for the disease is the most unfavorable: each patient faces death, and according to statistics, death occurs as a result of suffocation on average after three years.

Diagnostic methods

Paralysis is diagnosed visually based on obvious signs when a specialist realizes that the patient has no motor reflexes. But to determine the form and localization of the pathology, additional diagnostic measures are needed, which begin with checking the reflexes. Further procedures such as MRI, tomography, fluoroscopy and neurosonography are performed.

In case of Bell's palsy, when the limbs are not affected by pathological processes, a hearing test is first carried out, which allows us to identify the extent of the damage auditory nerve. Additionally, the vestibular apparatus is checked, a tear sample is taken, and a lumbar puncture is performed.

Treatment of paralysis with homeopathy

Paralysis is considered permanent in many cases, especially if it is caused by serious injury. However, in some cases, the patient can be raised to his feet, and not only methods of traditional medicine are used, but also homeopathic medicines. Even if such remedies are not always completely effective, they can increase the chance of recovery.

Among these means the following are used:

  • Caustikum (Caustikum) - a remedy that promotes recovery after lead poisoning leading to paralysis);
  • Conium (Conium) - help relieve paralyzed patients from involuntary tremors and seizures;
  • Bothrops (Botrops) - prescribed for Bell's palsy to speed up speech recovery;
  • Gelsemium – with complete or partial motor paralysis of the muscular system.

Paralysis

Causes and symptoms of paralysis

What is paralysis?

Paralysis is serious changes in the body, leading to loss and impairment of motor functions. In medicine, paralysis is characterized by the degree of manifestation, persistence and localization. There are complete and partial paralysis, irreversible and transient, widespread and non-common. When diagnosing paralysis in a place opposite to the site of the central nervous system lesion, it is called crossed or contralateral paralysis.

When the lesion is on the paralyzed side, they speak of uncrossed or ipsilateral paralysis. According to the degree and location, paralysis is divided into tetraplegia, monoplegia, hemiplegia and paraplegia. Hemiplegia is complete paralysis of the face or limbs on one side of the body. Diplegia is the name given to bilateral paralysis of one part of the body. Tetraplegia is diagnosed when all four limbs are paralyzed.

Paraplegia refers to partial or complete paralysis of both legs, combined with impaired motor functions of the lower body due to illness or injury. Many diseases of the human nervous system can be harbingers of paralysis. Paralysis does not exist separately as a disease and has many causal factors that cause it. Any disturbance in the functioning of the nervous system can lead to damage to motor functions.

Causes of paralysis

Among the organic causes that cause paralysis are: traumatic conditions, disseminated encephalomyelitis, infectious diseases (for example, viral encephalitis, various types of tuberculosis, inflammation of the meninges, poliomyelitis), poisoning of the body, metabolic disorders, nutritional disorders, vascular diseases, cancerous tumors.

Paralysis can be a consequence of hereditary or congenital diseases of the central nervous system. Toxic causes include: deficiency of vitamin B1 (beriberi disease), deficiency nicotinic acid(pellagra), alcoholic polyneuritis, intoxication of the body with salts of heavy metals (lead). Cerebral palsy (CP) and Erb's palsy are caused by a specific birth injury.

A list of diseases, the origin of which is unknown, can become harbingers of paralysis of various directions. Paralysis due to wounds and fractures occurs when there is a disruption of the motor pathways and centers. There are many cases where paralysis becomes a consequence of hysterics of a mentally ill person, then the patient needs the help of a psychiatrist.

Symptoms of paralysis

Clinically, some types of paralysis are distinguished, which act as an independent disease. For example, parkinsonism, polio, Erb's palsy, Bell's palsy, bulbar and pseudobulbar palsy, cerebral palsy, myoplegia, as well as many congenital and inherited diseases.

Peripheral facial paralysis is called Bell's palsy. It occurs when the facial nerve is damaged and is quite widespread. The causes of Bell's palsy are varied: hypothermia, polyneuropathy, infectious diseases (diphtheria, parotitis), cancerous tumors. The main symptoms of this disease are severe headaches and migraines.

The disease can result from injury or surgical manipulation of the body. But in many cases the origin of the disease is unknown. When the motor functions of the facial nerve are impaired, complete unilateral muscular paralysis of the face occurs. The patient cannot close his eyes, it is difficult for him to talk and eat. Bilateral damage to the facial nerve is very rare. Necrosis of muscles deprived of movement can occur after 2 weeks. The prognosis and further course of the disease are determined by the cause of the disease.

Thus, paralysis of the facial nerve due to ear disease or trauma may be irreversible. In many cases of facial paralysis, it is possible to restore the functions of the facial muscles after a few weeks.

A type of paralysis, bulbar palsy is of two types: acute or progressive. Poliomyelitis is a form of acute bulbar palsy. The disease disrupts the functioning of the medulla oblongata and pons, causing paralysis of the tongue and organs oral cavity. The onset of the disease is characterized by the following symptoms: headache, dizziness, fever. There is no muscle pain.

Bulbar palsy is characterized by the absence of a uniform pulse and breathing. The voice becomes nasal and sometimes it is difficult to understand what the patient is saying. The patient has difficulty keeping food in his mouth and spills it out. The presence of hemiplegia and monoplegia can often be noted. The course of the disease is rapid, death occurs within a few days. Recovery with partial paralysis is also possible.

The disease of progressive bulbar palsy varies in duration and occurs in middle-aged men. The origin of the disease is unknown. Progressive paralysis of the muscles of the oral cavity occurs. The symptoms are the same as for acute bulbar palsy. There is no treatment, so death occurs within 1 to 3 years.

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Diagnosis of paralysis

Diagnosis of paralysis should include the following points: a modern examination of the patient by a neurologist, examination of the body using highly efficient computed tomography, a full diagnosis of the disease using magnetic resonance imaging, checking leg reflexes (for example, the knee reflex), obtaining results using neurosonography, and fluoroscopy.

Various diagnostics for paralysis of motor functions of the body are carried out based on clinical signs and medical studies. The study of nerves in hemiplegia (paralysis of the face or limbs located on one side of the body) is important in establishing the location of the lesion. Such a serious disorder in the motor area of ​​the frontal lobe of the brain occurs along with complete paralysis of the symmetrical side.

Unilateral contraction of the facial muscles is a symptom of multiple sclerosis. If the cervical muscles are involved in the pathological process, then this may be indicated by the Lehr-Mitt symptom, which is manifested by a feeling of numbness and tingling in the hands and feet when the head is tilted.

Sometimes the patient experiences a sudden sharp pain when bending the neck, which spreads along the spine. When determining the location of the primary focus of a brain abscess, the auricles, mastoid processes and paranasal sinuses patient's nose.

When diagnosing Bell's palsy, hearing is tested to determine whether the auditory nerve is impaired, and the functioning of the vestibular system is also checked by monitoring the patient's balance, lacrimation is monitored, necessary blood tests are taken, and a lumbar puncture is performed.

Diagnosis of cerebral palsy involves monitoring the child during his or her first years of life. Differential diagnosis is aimed at identifying various congenital and hereditary diseases through scanning and various tests. When making a diagnosis of cerebral palsy, a thorough neurological examination is necessary.

Treatment of paralysis

The main task in treating paralysis is to eliminate the cause of the disease. In all cases, it is carried out specifically symptomatic treatment, gymnastics and therapeutic massage to help restore motor functions. For each case, the doctor individually selects a paralysis treatment program, including drug therapy.

Physical therapy is the main method of treating this dangerous disease. It is very important to position the affected limb correctly. In the case of central paralysis, the patient's arms and legs are positioned so that contractures do not appear. Gymnastics should combine energetic and passive movements. Passive exercises are carried out with great care, preventing excessive motor activity of the limbs.

For peripheral paralysis, a special massage is done before therapeutic exercises. When movements begin to appear, specific active actions are introduced into treatment. Brings great benefits physiotherapy in combination with a bath or swimming pool.

Special drug therapy is selected individually by a neurologist. Prozerin, dibazol, intramuscular injections of vitamin B1, melliktin (in case of increased muscle tone) are prescribed internally. In the treatment of dangerous Bell's palsy, salicylates, corticosteroids and, in addition to medicines– electrotherapy.

In the case of drug treatment of bulbar palsy, a course of vascular therapy is carried out using drugs that can improve metabolic processes brain, as well as oxygen therapy. Drugs used in the treatment of spastic paralysis: imidazoline, datrolene, gabaleptin benzodiazepines. In addition, for spastic paralysis, Botox treatment is used, injecting it into the affected muscles, which then become relaxed. Spastic paralysis is characterized by surgical intervention.

When treating paralysis, keeping the patient in bed for a long time can have a bad effect on the course of the disease. Bed rest will cause poor circulation, dizziness and fainting.

It is worth remembering one thing that when treating paralysis, you need to constantly move, and if this is an impossible task for the patient, then you need to help him. The practice of breathing exercises uses all the lungs, which do not work fully during paralysis.

Prevention of paralysis

Prevention of this disease consists mainly in the prevention of those serious diseases that can cause paralysis.

Paralysis of the tongue in humans

Tongue paralysis never occurs in isolation; it is always a symptom of some disease.

Boil a hard-boiled egg, cut it in half and immediately apply both halves while warm to the place where the pain is felt the most. When the egg cools down, the pain will go away and will not bother you for a long time.

Wolfberry, mustard, oak, mumiyo, radish.

Take fresh burdock (root, stem, leaves, inflorescences), wash, chop, and grind into a paste. Apply as a compress to the healthy side of the face. This remedy is effective only at the beginning of the disease.

Mix 1:1 black elderberry juice (or jam, jam from it) and good grape wine (preferably port). Take 3 tbsp. spoons 2 times a day before meals for 7 - 8 days.

Take 100 pcs. green pine cones (May), 25 leaves and flowers of rue and 1.5 kg of sugar, pour 2.5 liters of water and cook for 20 minutes, cool, strain. Take 1 tbsp. spoon 3 times a day before meals.

Place a few green leaves of indoor geranium on a linen napkin (it must be linen, since the flax hairs in it are the most important thing in treatment), bandage it on the sore spot, and tie a warm scarf on top. Replace the leaves with fresh ones 2-3 times, and after 2 hours the pain will go away.

Pour 1 cup of boiled water at room temperature into 4 teaspoons of crushed marshmallow roots and leave overnight. In the morning, take chamomile infusion into your mouth (1 teaspoon per 1 glass of boiling water) and keep it on the sore spot for as long as possible. At the same time, apply a gauze compress from marshmallow infusion to the outside of the sore spot, and on top of the gauze apply compress paper and woolen fabric (an old scarf or handkerchief). Apply the compress several times a day until the pain disappears. Marshmallow root can be replaced with flowers and leaves: in this case

2 tbsp. spoons of raw materials pour 1 glass of boiling water, leave for 1 hour.

If the muscles of the tongue are paralyzed, keep a tincture of wolfberry bark in your mouth for some time: 1 g of bark for 65 g of alcohol or vodka, leave for 21 days. Take 1 - 2 drops 3 times a day. THE PLANT IS POISONOUS!

For paralysis or paresis of the facial nerve, take an infusion of peony herb (Maryin root), collected at the beginning of flowering. Brew 2 teaspoons of herbs with 1 cup of boiling water, leave, wrapped, for 3 hours, strain. Drink 1 - 2 tbsp. spoons 3 times a day

3 - 4 weeks. At the same time, you need to take mumiyo (a piece of resin the size of a match head diluted in 20 ml of water) 30 minutes before meals.

Make an appointment with a doctor:

Paralysis is the loss of the ability to move at will. The most common causes of paralysis are stroke and injuries to the head, neck and spine.

Causes

Paralysis can also occur due to:

  • degenerative diseases of nerves and muscles (multiple sclerosis, myasthenia gravis, poliomyelitis, Parkinson's disease, Lou-Gehrig's disease);
  • tumors of the brain or spinal cord; infections of the nervous system (botulism, encephalitis).

Temporary paralysis can occur with Guillen-Barr syndrome, migraines, and seizures.

Types of paralysis

Doctors classify paralysis by location and severity:

  • paraplegia - paralysis of the legs;
  • quadriplegia - paralysis of the arms, legs and torso at the site of injury or abnormality of the spine;
  • hemiplegia - paralysis of one side of the body.

A paralyzed person cannot move at will or control the affected part of the body. Depending on the cause and type, the paralysis may be widespread or limited to one limb; temporary or permanent.

Some paralyzed people have uncontrollable muscle spasms (spastic paralysis) or completely relaxed muscles (flaccid paralysis).

Symptoms

With paralysis, other symptoms are possible:

  • headache;
  • visual impairment;
  • difficulty swallowing;
  • nausea and vomiting;
  • loss of control over urination and bowel movements;
  • muscle pain and weakness;
  • fatigue.

Sudden paralysis

If paralysis develops suddenly, seek medical help immediately. medical care. If you suspect a head, neck, or back injury, do not move the person unless their life is in danger, such as from fire or explosion. Wait until the professionals arrive.

To prevent further injury, stabilize the spine by keeping the victim's head in line with the body. To do this, use blankets, towels, and clothes, placing them on the sides, near the victim’s head and neck.

Do not give the victim anything to drink.

If you suspect a head, neck, or back injury, do not move the victim.

What doctors are doing

Emergency doctors immobilize the spine, take measures to reduce the pressure inside the skull, and administer oxygen. A breathing tube may be inserted into the patient.

A ventilator may be used in the hospital. Research is being done to determine the cause of the paralysis.

If the cranial nerves that control eye movements, tongue movements, facial expression, swallowing, and other important functions are paralyzed, the patient may have difficulty swallowing. To avoid exhaustion, he is prescribed liquid and soft foods, feeding through a tube or intravenously.

Maintaining muscle tone and joint function

To maintain muscle tone in paralyzed limbs, the arms and legs must be subjected to special exercises daily.

To avoid abnormal joint position, called contracture, splints are placed on paralyzed limbs. Special devices are used if the patient cannot raise the foot and it hangs down.

Bedsores can be minimized by changing the patient's position frequently and taking good care of the skin.

Preventing Lung Problems

Your doctor may prescribe physical therapy for your chest. It includes special postures, tapping, vibration, as well as coughing and deep breathing exercises.

This helps the patient:

  • cough up pulmonary secretions;
  • expand the lungs;
  • more effectively use the muscles that provide breathing.

As you recover, physical, speech, and occupational therapy can help you overcome specific difficulties.

What else do you need to know

Long-term paralysis can cause complications associated with immobility, causing damage to muscles, joints, skin and lungs. Careful daily care is necessary to prevent or minimize these complications.

A single center for making appointments with a doctor by phone.

Progressive bulbar palsy is a gradually developing dysfunction of the bulbar group of caudal cranial nerves, caused by damage to their nuclei and/or roots. A triad of symptoms is characteristic: dysphagia, dysarthria, dysphonia. The diagnosis is made based on examination of the patient. Additional examinations (cerebrospinal fluid analysis, CT, MRI) are carried out to determine the underlying pathology that caused the bulbar palsy. Treatment is prescribed in accordance with the causative disease and existing symptoms. May be required urgent measures: resuscitation, mechanical ventilation, combating heart failure and vascular disorders.

Progressive bulbar palsy

Bulbar palsy occurs when the nuclei and/or roots of the bulbar group of cranial nerves located in the medulla oblongata are damaged. The bulbar nerves include the glossopharyngeal (IX pair), vagus (X pair) and hypoglossal (XII pair) nerves. The glossopharyngeal nerve innervates the muscles of the pharynx and provides its sensitivity, is responsible for taste sensations posterior 1/3 of the tongue, provides parasympathetic innervation to the parotid gland. The vagus nerve innervates the muscles of the pharynx, soft palate, larynx, upper sections digestive tract and respiratory tract; gives parasympathetic innervation of internal organs (bronchi, heart, gastrointestinal tract). The hypoglossal nerve provides innervation to the muscles of the tongue.

In clinical neurology, acute and progressive bulbar palsy, unilateral and bilateral nature of the lesion are distinguished. Acute paralysis occurs suddenly due to an acute disorder cerebral circulation(stroke in the vertebrobasilar region), neuroinfection (polyseasonal encephalitis, lethargic encephalitis, etc.), acute intoxication, compression of the medulla oblongata (hematoma, bone fragment from a fracture of the 1st cervical vertebra), dislocation syndrome developed as a result of edema of the brain and masses -effect. Progressive bulbar palsy is characterized by a gradual increase in symptoms and is observed in various progressive diseases of the central nervous system.

Causes of progressive bulbar palsy

Damage to the nuclei of the bulbar nerves in the medulla oblongata or their roots at the exit from it is secondary and is a consequence of CNS lesions of different nature and etiology. Progressive bulbar palsy is often observed with motor neuron diseases (Kennedy amyotrophy, amyotrophic lateral sclerosis), infectious lesions of the central nervous system ( tick-borne encephalitis, bulbar form of poliomyelitis, neurosyphilis), volumetric processes of the posterior cranial fossa (cerebellar tumors, gliomas, ependymomas, metastatic brain tumors, tuberculoma, cystic formations), demyelinating diseases (EM, multiple sclerosis).

The cause of bulbar palsy may be chronic cerebral ischemia, which develops as a result of atherosclerosis or chronic vascular spasm in hypertension. Rare factors causing damage to the bulbar group of cranial nerves include craniovertebral anomalies (primarily Chiari malformation) and severe polyneuropathies (Guillain-Barré syndrome).

Symptoms of progressive bulbar palsy

At the core clinical manifestations Bulbar palsy is a peripheral paresis of the muscles of the pharynx, larynx and tongue, which results in disturbances in swallowing and speech. The basic clinical symptom complex is a triad of signs: swallowing disorder (dysphagia), articulation disorder (dysarthria) and speech sonority (dysphonia). Difficulty swallowing food begins with difficulty taking liquids. Due to paresis of the soft palate, fluid from the oral cavity enters the nose. Then, with a decrease in the pharyngeal reflex, swallowing disorders of solid foods develop. Limitation of tongue mobility leads to difficulty chewing food and moving the food bolus in the mouth. Dysarthria is characterized by slurred speech and a lack of clarity in the pronunciation of sounds, which makes the patient’s speech incomprehensible to others. Dysphonia manifests itself as hoarseness of voice. Nasolalia (nasality) is noted.

The patient's appearance is characteristic: the face is hypomimic, the mouth is open, there is drooling, difficulty chewing and swallowing food, and food falling out of the mouth. Due to damage to the vagus nerve and disruption of the parasympathetic innervation of somatic organs, disorders of respiratory function, heart rate and vascular tone occur. These are the most dangerous manifestations of bulbar palsy, since often progressive respiratory or heart failure causes the death of patients.

When examining the oral cavity, atrophic changes in the tongue, its folding and unevenness are noted, and fascicular contractions of the tongue muscles may be observed. The pharyngeal and palatal reflexes are sharply reduced or not evoked. Unilateral progressive bulbar palsy is accompanied by drooping of half of the soft palate and deviation of its uvula to the healthy side, atrophic changes in 1/2 of the tongue, deviation of the tongue towards the affected side when it protrudes. With bilateral bulbar palsy, glossoplegia is observed - complete immobility of the tongue.

Diagnosis of progressive bulbar palsy

A neurologist can diagnose bulbar palsy by carefully studying the patient’s neurological status. The study of the function of the bulbar nerves includes assessment of the speed and intelligibility of speech, timbre of voice, volume of salivation; examination of the tongue for the presence of atrophies and fasciculations, assessment of its mobility; examination of the soft palate and checking the pharyngeal reflex. It is important to determine the respiratory rate and heart rate, and study the pulse to detect arrhythmia. Laryngoscopy allows you to determine the lack of complete closure of the vocal cords.

During diagnosis, progressive bulbar palsy must be distinguished from pseudobulbar palsy. The latter occurs with supranuclear damage to the corticobulbar tracts connecting the nuclei of the medulla oblongata with the cerebral cortex. Pseudobulbar palsy is manifested by central paresis of the muscles of the larynx, pharynx and tongue with hyperreflexia (increased pharyngeal and palatine reflexes) and increased muscle tone characteristic of all central paresis. Clinically it differs from bulbar palsy in the absence of atrophic changes in the tongue and the presence of oral automatism reflexes. Often accompanied by violent laughter resulting from spastic contraction of the facial muscles.

In addition to pseudobulbar palsy, progressive bulbar palsy requires differentiation from psychogenic dysphagia and dysphonia, various diseases with primary muscular damage causing myopathic paresis of the larynx and pharynx (myasthenia gravis, Rossolimo-Steinert-Kurshman myotonia, paroxysmal myoplegia, oculopharyngeal myopathy). It is also necessary to diagnose the underlying disease that led to the development of bulbar syndrome. For this purpose, cerebrospinal fluid, CT and MRI of the brain are examined. Tomographic studies make it possible to visualize brain tumors, demyelination zones, cerebral cysts, intracerebral hematomas, cerebral edema, displacement of cerebral structures during dislocation syndrome. CT or radiography of the craniovertebral junction can reveal abnormalities or post-traumatic changes in this area.

Treatment and prognosis of progressive bulbar palsy

Treatment tactics for bulbar palsy are based on the underlying disease and leading symptoms. In case of infectious pathology, etiotropic therapy is carried out; in case of cerebral edema, decongestant diuretics are prescribed; in case of tumor processes, the issue of removing the tumor or performing shunt surgery to prevent dislocation syndrome is decided together with a neurosurgeon. Unfortunately, many diseases in which bulbar syndrome occurs are a progressive degenerative process occurring in cerebral tissues and do not have effective specific treatment. In such cases, symptomatic therapy is carried out to support the vital functions of the body. Thus, in case of severe respiratory disorders, tracheal intubation is performed and the patient is connected to a ventilator; in case of severe dysphagia, tube feeding is provided; vascular disorders are corrected with the help of vasoactive drugs and infusion therapy. To reduce dysphagia, neostigmine, ATP, and vitamins are prescribed. B, glutamic acid; for hypersalivation - atropine.

Progressive bulbar palsy has a highly variable prognosis. On the one hand, patients may die from cardiac or respiratory failure. On the other hand, when successful treatment underlying disease (for example, encephalitis), in most cases patients recover with full restoration swallowing and speech function. Due to the lack of effective pathogenetic therapy, bulbar palsy associated with progressive degenerative damage to the central nervous system (with multiple sclerosis, ALS, etc.) has an unfavorable prognosis.

Paralysis

Symptoms of paralysis

  • Complete absence of muscle strength in any muscle or muscle group (for example, in the extensors of the fingers, neck muscles) and related phenomena:
    • change in gait (with a complete absence of muscle strength in the pelvic girdle) - the gait becomes similar to a “duck”, waddling from foot to foot;
    • foot drop when lifting the leg (in the complete absence of muscle strength of the extensor muscles of the foot). At the same time, a “chasing” or “cock” gait develops, that is, with each step a person tries to raise his foot higher so as not to touch the ground with his foot;
    • hanging head forward (with a complete lack of muscle strength in the back muscles of the neck);
    • complete lack of muscle strength in the arm muscles;
    • weakness in the leg muscles and the associated inability to walk, difficulty getting up from a sitting position.
  • Traffic violation eyeballs: the eye/both eyes do not rotate in one or more directions, which leads to a violation of coordinated eye movements and the development of strabismus.
  • The abduction of both eyes to one side (associated with dysfunction of coordinated gaze) is the so-called “gaze paralysis.”
  • Nasality, slurred speech (with a nasal tint) - with paralysis of the muscles of the soft palate.
  • Sluggishness of the tongue, deviation of the tongue when sticking it out of the mouth - with weakness of the muscles of the tongue.

Forms

  • Depending on the origin of paralysis, there are two forms:
    • central (spastic) is associated with disorders of higher motor motor neurons (nerve cells that provide muscle movement), combined with an increase in tone in paralyzed muscles;
    • peripheral (flaccid) is associated with damage to motor neurons or nerves going to the muscles, combined with a decrease in tone in paralyzed muscles and their thinning (atrophy).
  • Depending on the prevalence of lack of muscle strength in the limbs, the following forms of paralysis are distinguished:
    • monoplegia - in one limb;
    • hemiplegia - in the limbs on one side;
    • paraplegia - only in the arms or only in the legs;
    • tetraplegia - in all limbs.

Causes

  • Acute disturbance of cerebral or spinal circulation (stroke), including hemorrhage.
  • Tumors of the brain and spinal cord.
  • Brain and spinal cord injuries.
  • Abscess (ulcer) of the brain and spinal cord.
  • Inflammation of the brain (encephalitis) or spinal cord (myelitis).
  • Demyelinating diseases accompanied by the breakdown of myelin (a protein that ensures rapid transmission of nerve impulses along fibers), for example, multiple sclerosis (a disease in which many small foci of demyelination form in the brain and cerebellum), disseminated encephalomyelitis (a disease of a presumably infectious nature in which Many foci of demyelination form in the brain and cerebellum).
  • Poisoning: salts of heavy metals, industrial poisons, nerve poisons, alcohol.
  • Immune-inflammatory diseases, for example, Guillain-Barre syndrome, manifested by the absence of reflexes (detected when neurological examination), decreased muscle strength and breathing problems (weakness of the respiratory muscles).
  • Myasthenia gravis is a disease characterized by pathological muscle fatigue, with repeated movements increasing muscle weakness, which partially or completely goes away after rest.
  • Botulism is a disease associated with poisoning by botulinum toxin produced by the bacterium Clostridium botulinum. It also manifests itself as breathing problems, slurred speech, ptosis (drooping) of the upper eyelid, diarrhea (diarrhea) and abdominal pain.
  • Myopathies are diseases associated with congenital or acquired metabolic disorders in muscles.
  • Epilepsy is a disease characterized by the presence of a so-called epileptogenic focus in the brain: it periodically spontaneously generates an electrical discharge, disrupting the functioning of the brain.
  • Diseases of motor neurons (nerve cells that provide muscle movement), for example, amyotrophic lateral sclerosis (manifested by a gradual increase in weakness in the muscles of the trunk, limbs and respiratory muscles), spinal muscular atrophy (hereditary diseases characterized by the gradual death of motor neurons).

A neurologist will help in treating the disease

Diagnostics

  • Analysis of complaints and medical history:
    • how long ago there was a lack of strength in any muscle group (arms, legs, neck);
    • what immediately preceded the appearance of complaints (consumption of canned foods, diarrhea (diarrhea), severe headache, fever);
    • did anyone in the family have similar complaints;
    • whether the patient’s profession or place of residence is associated with exposure to harmful substances (heavy metal salts, organic solvents).
  • Neurological examination: assessment of muscle strength on a 5-point scale, search for other symptoms of neurological pathology (facial asymmetry, lack of reflexes, muscle thinning (atrophy), strabismus, swallowing disorders).
  • Blood test: may detect signs of inflammation in the blood (increased erythrocyte sedimentation rate (red blood cells), number of white blood cells), increased muscle metabolic products (creatine kinase).
  • Toxicological blood test: detection of signs of poisoning.
  • Prozerin test: allows you to identify myasthenia gravis (a disease characterized by pathological muscle fatigue), in which the administration of this drug quickly restores muscle strength.
  • ENMG (electroneuromyography): the method allows you to evaluate the electrical activity of muscles, the speed of nerve impulses along nerve fibers, and conduction blocks.
  • EEG (electroencephalography): this method evaluates the electrical activity of different parts of the brain, which changes in various diseases.
  • CT (computed tomography) and MRI (magnetic resonance imaging) of the head and spinal cord make it possible to study the structure of the brain and spinal cord layer by layer, identify violations of the structure of its tissue, and also determine the presence of ulcers, hemorrhages, tumors, and foci of decay of nervous tissue.
  • MRA (magnetic resonance angiography): the method allows you to evaluate the patency and integrity of the arteries in the cranial cavity, as well as detect brain tumors.
  • A consultation with a neurosurgeon is also possible.

Treatment of paralysis

  • Treatment should be aimed at the cause of the paralysis.
    • Surgical treatment of the brain or spinal cord:
      • tumor removal;
      • removal of hemorrhage;
      • removal of the abscess, antibacterial therapy.
    • Normalization of arterial (blood) pressure and drugs that improve cerebral blood flow and metabolism (angioprotectors, nootropics) for cerebrovascular disorders.
    • Antibiotic therapy for infectious lesions of the brain or spinal cord.
    • Administration of anti-botulinum serum for botulism (a disease associated with poisoning by botulinum toxin produced by the bacterium Clostridium botulinum).
    • Drugs that improve neuromuscular conduction in myasthenia gravis (a disease characterized by pathological muscle fatigue).
    • Drugs that improve nutrition and restoration of nervous tissue (neurotrophic drugs).
    • Treatment of poisoning (administration of solutions, vitamins B, C, A).
  • Development of paralyzed muscles, since prolonged absence of muscle function leads to irreversible loss of muscle function.

Complications and consequences

  • A persistent neurological defect in the form of a decrease or absence of muscle strength in any muscle group (arms, legs, neck).
  • Contractures (irreversible hardening of muscles) and ankylosis of joints (formation of joint immobility).

Prevention of paralysis

  • Timely treatment of infectious diseases.
  • Quitting bad habits (smoking, alcohol).
  • Maintaining healthy image life (regular walks for at least 2 hours, physical exercise, adherence to a day and night routine (night sleep for at least 8 hours)).
  • Compliance with the diet and diet (regular meals at least 2 times a day, inclusion in the diet of foods rich in vitamins: fruits, vegetables).
  • Timely consultation with a doctor if health problems arise.
  • Control of arterial (blood) pressure.

Additionally

  • In addition to skeletal muscle paralysis in the usual sense of the word, the concepts of “gaze palsy” and “soft palate palsy” are sometimes used.
  • Sometimes the term “paralysis” is used to describe a violation of muscle contraction, the strength of which cannot be measured quantitatively (for example, on a 5-point scale). This situation occurs, for example, when the contraction of the soft palate is impaired.
  • Sources

Paul W. Brazis, Joseph K. Masdew, Jose Biller - Topical diagnosis in clinical neurology, 2009

Brilman J. – Neurology, 2007

G.A.Akimov, M.M.Odinak - Differential diagnosis of nervous diseases, 2001

M. Mumenthaler - Differential diagnosis in neurology, 2010

Nikiforov A.S. – Clinical neurology, vol. 2, 2002

Paralysis symptoms and treatment | Forms and causes of paralysis

Paralysis is a disorder of voluntary movements caused by a violation of the innervation of muscles, which can manifest itself as the absence or disturbance of spontaneous movements or a decrease in muscle strength. Let's take a closer look at what paralysis is, symptoms and treatment, forms and causes of paralysis.

Paralysis - symptoms of the disease

Symptoms of paralysis can be expressed in the inability to perform a movement with the resistance of the doctor’s hand or to hold a certain position for a long time (for example, outstretched arms or raised legs) in the Barre test.

Diagnostic symptoms of paralysis

Paralysis is diagnosed using a 5-point system:

  • 5 – normal muscle strength,
  • 4 – strength is reduced, but the patient with symptoms of paralysis makes active movements, overcoming the resistance of the doctor’s hand,
  • 3 – a patient with symptoms of paralysis is able to carry out movements against gravity, but not against a resisting hand,
  • 2 – the patient is not able to resist gravity,
  • 1 – minimal active movements are possible,
  • 0 – no active movements.

Differential symptoms of paralysis

It is important to distinguish the symptoms of paralysis from restrictions of movement due to pain syndromes, joint contractures or tendon injuries. In most of these cases, in contrast to paralysis, both active and passive movements are difficult.

The acute development of hemiplegia or tetraplegia in a young woman, especially after stress and in cases where no convincing reasons for this condition are found, makes one think about the possibility of hysteria. Hysterical pseudo-paralysis is characterized by the absence of paresis of facial muscles. Weakness in pseudoparalysis often involves the entire limb rather than individual muscle groups and may be accompanied by a paradoxical combination of muscle hypotonia and hyperreflexia. When checking strength, its “stepwise” decrease is often detected (the patient jerks “yields” to the doctor’s effort), and when performing passive movements, one can notice the resistance of “paretic” muscles. “Trying” to lift the “paretic” leg, patients do not rely on the heel of the healthy leg (to fix this, the doctor first places his hand under it).

When raising a healthy leg, the heel of the “paretic” leg usually presses down, but then the patient cannot, due to “weakness,” reproduce this movement on command. When lowering the “paretic” arm in the Barre test, it does not rotate inward (with pyramidal paresis, the pronators are always stronger than the supinators). Pseudo-paralysis is often accompanied by other hysterical symptoms(transient mutism, blindness, deafness, etc.).

Forms of paralysis

The terms “paralysis” and “plegia” mean a complete absence of active movements, the term “paresis” means a partial loss of muscle strength. The prefix "hemi-" means the involvement of only the right or only the left limbs, "para" - the upper or, more often, lower limbs, "tetra" - all four limbs.

There are 2 main types of paralysis: central paralysis (the cause of which is damage to the central motor neurons, the bodies of which lie in the motor zone of the cortex, and long axons follow as part of the pyramidal tract to the anterior horns of the spinal cord) and peripheral paralysis (the cause of which is damage to peripheral motor neurons, the bodies of which lie in the anterior horns of the spinal cord, and the axons follow as part of the roots, plexuses, and nerves to the muscles).

Symptoms of central paralysis

Symptoms of central spastic paralysis occur in most vascular, traumatic and infectious diseases of the brain and spinal cord (if the focus of the spinal lesion is located above the lumbar enlargement), as well as in multiple sclerosis.

Cerebral lesions are characterized by central mono- or hemiparesis, spinal lesions are characterized by lower paraparesis, and less commonly, tetraparesis.

Symptoms of peripheral paralysis

Symptoms of peripheral paralysis are observed in diseases and injuries of peripheral nerves and plexuses, spondylogenic lumbosacral and cervicobrachial radiculitis, lesions of the spinal cord at the level of the lumbar enlargement and below it, with some brain lesions (central flaccid paralysis) and hereditary diseases of the nervous system ( myopathies, amyotrophies). Movement disorders are often localized in the area of ​​innervation of the corresponding roots, plexuses or nerves; with spinal lesions, lower paraparesis is observed, with diseases of the brain - hemiparesis, myopathies - symmetrical disorders on the trunk and in the proximal parts of the extremities, and with amyotrophies and polyneuritis - in the distal parts.

IN acute stage distinguishing central and peripheral forms of paralysis can be difficult, since in both cases muscle hypotonia and decreased reflexes are observed, and only subsequently, as a rule (but not always), spasticity, hyperreflexia and clonus characteristic of central paresis appear. More reliable symptoms of central paralysis are pathological foot reflexes, peripheral paralysis is early loss of reflexes, rapidly developing atrophy and fasciculations (with damage to the anterior horns).

Muscle weakness in primary muscle diseases (myopathies) and disorders of neuromuscular transmission (myasthenia gravis) approaches peripheral paralysis in its characteristics.

Afferent form of paralysis

Symptoms of afferent paralysis are peculiar disorders of coordination of movements, as a result of which the latter lose coherence, accuracy, smoothness, become slow and often do not reach the goal. The ability to work and self-care of patients with this form of paralysis are sharply reduced, even while maintaining voluntary movements and sufficient muscle strength.

The performance of subtle differentiated actions is especially impaired. The afferent form of paralysis occurs when there is a disorder (or loss) of muscle-articular sensation as a result of damage to the brain (especially the parietal lobe or visual thalamus) or the spinal cord (posterior columns or dorsal horns).

With a focus in the cerebral cortex, symptoms of paralysis of the form afferent monoparesis are more often observed; thalamic lesions lead to the formation of afferent hemiparesis with characteristic intense pain, and spinal lesions lead to afferent paraparesis.

Hemiparesis as a form of paralysis

This form of paralysis is usually central in nature and occurs when the brain is affected. Possible causes of paralysis of this form:

Bulbar syndrome

Dysfunction of the cranial nerves, the nuclei of which are located in the medulla oblongata, is called bulbar syndrome. The main characteristic of the disease is general paralysis of the tongue, muscles of the pharynx, lips, epiglottis, vocal cords and soft palate. Often the consequence of bulbar syndrome (paralysis) is a disorder speech apparatus, functions of swallowing, chewing and breathing.

A less pronounced degree of paralysis is manifested in cases of unilateral damage to the nuclei of the IX, X, XI and XII (caudal group) nerves, their trunks and roots in the medulla oblongata, but a severe degree of bulbar syndrome is more common with bilateral damage to the same nerves.

Pseudobulbar syndrome is a bilateral interruption of the corticonuclear pathways, leading to a neurological syndrome. It has a similar clinical picture to bulbar syndrome, but has a number of distinctive features and occurs due to damage to other parts and structures of the brain.

A significant difference between bulbar and pseudobulbar syndrome is that in the second there is no disturbance in the rhythm of cardiac activity, atrophy of paralyzed muscles, or cessation of breathing (apnea). It is often accompanied by unnatural forced laughter and crying of the patient, resulting from a disruption of the connection between the central subcortical nodes and the cerebral cortex. Most often, pseudobulbar syndrome occurs with diffuse brain lesions of traumatic, vascular, intoxication or infectious origin.

Bulbar syndrome: causes

Scroll possible reasons The origin of paralysis is quite wide, it includes genetic, vascular, degenerative and infectious factors. Thus, genetic causes include acute intermittent porphyria and Kennedy bulbospinal amyotrophy, and degenerative causes include syringobulbia, Lyme disease, polio and Guillain-Barre syndrome. The cause of bulbar syndrome can also be a stroke of the medulla oblongata (ischemic), which is much more likely than other diseases to lead to death.

The development of bulbar syndrome occurs with amyotrophic lateral sclerosis, paroxysmal myoplegia, spinal amyotrophy Fazio-Londe, diphtheria, post-vaccination and paraneoplastic polyneuropathy, as well as due to hyperthyroidism.

Other probable causes of bulbar syndrome include diseases and processes in the posterior cranial fossa, brain and craniospinal region, such as:

  • Botulism;
  • Tumor in the medulla oblongata;
  • Bone abnormalities;
  • Syringobulbia;
  • Granulomatous diseases;
  • Meningitis;
  • Encephalitis.

Against the background of paroxysmal myoplegia, myasthenia gravis, dystrophic myotonia, oculopharyngeal myopathy, Kearns-Sayre syndrome, psychogenic dysphonia and dysphagia, paralysis can also develop.

Symptoms of bulbar syndrome

With paralysis, patients have problems with the consumption of liquid food, they often choke on it, and sometimes they cannot reproduce swallowing movements, which is why saliva may flow from the corners of their mouth.

In particularly severe cases of bulbar syndrome, a disorder of cardiovascular activity and respiratory rhythm may occur, which is due to the close location of the nuclei of the cranial nerves of the caudal group with the centers of the respiratory and cardiovascular systems. Such involvement in pathological process cardiac and respiratory systems often leads to death.

A sign of bulbar syndrome is loss of the palatal and pharyngeal reflexes, as well as atrophy of the tongue muscles. This occurs due to damage to the nuclei of the IX and X nerves, which are part of the reflex arcs of the above reflexes.

The most common symptoms of bulbar syndrome are the following:

  • The patient lacks facial expressions, he cannot swallow or chew food fully;
  • Violation of phonation;
  • Getting liquid food into the nasopharynx after consumption;
  • Heart dysfunction;
  • Nasal and slurred speech;
  • In the case of unilateral bulbar syndrome, there is a deviation of the tongue to the side unaffected by paralysis, its twitching, as well as drooping of the soft palate;
  • Breathing disorders;
  • Absence of palatine and pharyngeal reflex;
  • Pulse arrhythmia.

Symptoms of paralysis in each individual case can be of varying degrees of severity and complexity.

Diagnosis of bulbar syndrome

Before proceeding with direct treatment, the doctor must examine the patient, especially the oropharynx area, identify all the symptoms of the disease, and conduct an electromyography, according to which it is possible to determine the severity of paralysis.

Treatment of bulbar syndrome

In some cases, to save the life of a patient with bulbar syndrome, preliminary urgent Care. The main goal of such assistance is to eliminate the threat to the patient’s life before he is transported to a medical facility, where adequate treatment will then be selected and prescribed.

The doctor, depending on the clinical symptoms and the nature of the pathology, can predict the outcome of the disease, as well as the effectiveness of the proposed treatment for bulbar syndrome, which is carried out in several stages, namely:

  • Resuscitation, support of those body functions that were impaired due to paralysis - artificial ventilation to restore breathing, the use of Proserin, adenosine triphosphate and vitamins to trigger the swallowing reflex, the appointment of Atropine to reduce salivation;
  • This is followed by symptomatic therapy aimed at alleviating the patient’s condition;
  • Treatment of the disease against which the development of bulbar syndrome occurred.

Patients with paralysis are fed enterally, using a feeding tube.

Bulbar syndrome is a disease that occurs due to disruption of the cranial nerves. Often, even with adequate treatment, it is possible to achieve 100% recovery of the patient only in isolated cases, but it is quite possible to significantly improve the patient’s well-being.

If a child was injured in utero or suffered a birth injury, special attention should be paid to his speech.

We continue to introduce readers to various speech disorders with the help of L. Paramonova’s book “Speech Therapy for Everyone.” in general and in particular we have already talked. Today we will talk about dysarthria.

Dysarthria is a disorder of the sound pronunciation side of speech, which is caused by an organic lesion central department speech motor analyzer and associated disruption of the innervation of speech muscles. The term “dysarthria” itself means “a disorder of articulate speech” (“arthron” translated into Russian means “articulation”, and “diz” means “disorder”). The prevalence of dysarthria among mentally normal children ranges from 3 to 6%, but these figures have a clear upward trend.

Dysarthria most often is not an independent speech disorder, but is only one of the symptoms of a serious illness, which is usually congenital or occurs before the age of two years. Depending on the location of the brain lesion, dysarthria manifests itself in different ways, and therefore there are several types of it, which are inappropriate to consider here due to the impossibility of practical use of this information by non-specialists.

With complete paralysis of the articulatory muscles, anarthria occurs - a complete absence of pronunciation in the child. The main manifestations of severe dysarthria will be discussed further. But so-called erased dysarthria can often be observed, which needs to be discussed in a little more detail, since it is very widespread and, moreover, can be difficult to distinguish from dyslalia.

Erased dysarthria

Erased dysarthria is based on very small, literally pinpoint organic lesions of the cerebral cortex. Their presence leads to paresis of only certain small groups of articulatory muscles (for example, only the tip of the tongue or only one side of it). Under such conditions, the child suffers from the pronunciation of only individual sounds at an almost normal rate and rhythm of speech and in the absence of pronounced disorders of speech breathing and voice.

For a long time, such disorders in the pronunciation of sounds were classified as functional motor dyslalia, without noticing their specificity. However, the difficulties of overcoming them forced specialists to study this issue more carefully, as a result of which erased dysarthria was separated from the group of functional motor dyslalia. (During a neurological examination, paresis of individual articulatory muscles was discovered in these children, leading to definite disturbances in the pronunciation of sounds.)

Sound pronunciation disorders with erased dysarthria have not only a different causality compared to dyslalia, but also a different external manifestation. In particular, erased dysarthria is characterized by interdental pronunciation of sounds associated with weakness (pareticity) of the muscles of the tip of the tongue - it simply cannot be held behind the teeth. Often there is a “lateral” pronunciation of some consonants, which is associated with paresis of one side of the tongue. In these cases, the tongue, when protruding from the mouth, usually deviates to one side, and when articulating some sounds it becomes an “edge” in the mouth, which contributes to the lateral leakage of air. Such disturbances in the pronunciation of sounds at any age cannot be attributed to age-related peculiarities of sound pronunciation due to their being due to pathological reasons. Erased dysarthria never goes away with age, as evidenced by its presence in many adults.

Causes of cerebral palsy and dysarthria

The causes of cerebral palsy, and therefore the causes of dysarthria, are organic lesions of the child’s nervous system, which can occur in utero, during childbirth or as a result of early childhood diseases (meningitis, meningoencephalitis, traumatic lesions or vascular disorders).

Until relatively recently, the main cause of cerebral palsy (and therefore dysarthria) was considered to be birth trauma, causing cerebral hemorrhage, birth asphyxia and other complications during childbirth. However, it has now become clear that in more than 80-90% of cases, damage to the fetal nervous system occurs in utero. It is the insufficient usefulness of the fetus and its “unpreparedness” for active participation in the process of childbirth that leads to its complicated course and possible additional brain damage. These injuries can be the result of cesarean section, asphyxia at birth, or birth trauma during the provision of mechanical assistance, which is a forced means and is used only in cases of extreme necessity. Knowledge of this circumstance is extremely important both from the point of view of preventing cerebral palsy and, in most cases, the dysarthria that accompanies it.

If the main reason for the occurrence of both is not “for some unknown reason” that labor is so difficult, then the main content of prevention should be concern for the normal course of pregnancy, which very much depends on the seriousness of the woman’s attitude towards this most important period of her life. It has full power to exclude such harmful intrauterine development fetus, but, nevertheless, often present pathogenic factors, such as smoking and drinking alcoholic beverages even during pregnancy, constant overwork and non-compliance with a healthy daily routine, continued work in hazardous industries and on the night shift, lifting heavy objects and generally having large physical activity, “emergency” flights and transfers to other cities or even to other continents almost before the birth itself, which in such cases often begin right on the road and therefore, in principle, cannot proceed normally.

Speech and non-speech symptoms of dysarthria

Speech symptoms. The speech of children suffering from a severe form of dysarthria actually loses its articulation and becomes almost incomprehensible to others (“like porridge in the mouth”). What's the matter here? As previously noted, motor commands from the central part of the speech motor analyzer to the peripheral speech organs are transmitted along nerve pathways. With organic damage to these speech parts of the brain or directly to the motor nerves, full transmission of nerve impulses becomes impossible, and phenomena of paralysis or paresis develop in the muscles themselves. And since these paresis can spread not only to the muscles of the tongue and lips, but also to the muscles of the soft palate, vocal cords and respiratory organs, with dysarthria not only the articulation of sounds is impaired, but also voice formation and speech breathing.

With severe paresis of the tongue, the articulation of almost all speech sounds, including vowels, suffers. Paresis of the soft palate causes the appearance of a nasal tone of voice, paresis of the vocal cords causes a disturbance in the process of voice formation and a change in voice timbre, paresis of the respiratory muscles causes a dysfunction of speech breathing, which becomes superficial and arrhythmic, and therefore does not provide a full air stream for voice formation.

In addition to impaired motor function of the speech muscles due to the presence of paralysis and paresis, the sensitivity of these muscles also suffers, and therefore the child does not feel the position of his articulatory organs well enough. For this reason, it is difficult for him to find the necessary articulations, which creates additional difficulties both in mastering sound pronunciation and in correcting it.

All this taken together leads to the fact that dysarthria, in its external manifestations, differs sharply from dyslalia. So, if with dyslalia (with the exception of mechanical dyslalia due to congenital cleft palates) defects in sound pronunciation appear against the background of normal tempo and rhythm of speech, normal speech breathing and voice formation, then with dysarthria there is a picture of a general phonetic disadvantage of speech as a whole, as a result of which it loses its intelligibility, articulation.

Constantly hearing a child's own slurred speech in many cases leads to the appearance of secondary disorders of auditory differentiation of sounds.

The imperfection of auditory differentiation of sounds, in turn, secondarily causes difficulties in mastering the phonemic analysis of words.

Poor orientation in the sound composition of speech, associated with impaired auditory differentiation of sounds and difficulties in phonemic analysis of words, inevitably leads to the appearance of specific writing disorders in children - corresponding types of dysgraphia.

Difficulty and insufficiency verbal communication Secondarily, it may also be due to the poverty of the child’s vocabulary and the unformation of his grammatical structure of speech.

Thus, with severe dysarthria, speech suffers primarily or secondarily, in fact, in all its links, and not just in relation to sound pronunciation itself.

Non-speech symptoms. Dysarthria against the background of cerebral palsy is characterized by the presence of not only the speech symptoms discussed above, but also a number of non-speech symptoms, which ultimately also, in one way or another, make it difficult to master speech. These symptoms include the following.

  1. Paralysis and paresis of the muscles of the limbs and torso. Paresis of the legs sharply limits (or even completely eliminates) the child’s ability to move in space, which disrupts the development of his visual-spatial concepts, since he perceives space by the measure of his own steps. Otherwise, he cannot even judge the degree of distance from him of certain objects, so it is not by chance that a child who has not yet mastered the skill of walking tries to reach the moon from the sky, stretching out his little hand to it - it seems to him that it is very close.
    Paralysis and paresis of the hands limit (or exclude) the possibility of manipulating objects, which in the second year of a child’s life plays a decisive role in his knowledge of the world around him (the activity of the “cognitive hand”). Holding various toys in his hands, and also often bringing them to his mouth and trying to lick and even “taste” them, the child gradually gets an idea of ​​their shape, size, smoothness or roughness of the surface, temperature, which is different for cold metal objects and much warmer wooden ones. and plush, etc.

  2. It is quite understandable that if in his sensory experience a child has not received an idea of ​​the spatial and other characteristics of objects, then he will also have difficulty in verbally denoting these characteristics. It will be very difficult for him not only to express in words what is further and what is closer, which object is higher and which is lower, etc., but even to understand these spatial relationships between objects.
  3. Commonly observed paresis oculomotor muscles. With paresis of these muscles, the child is impaired in such important visual functions as fixing the gaze on an object, “feeling” it with the gaze, “tracing” a moving object with the eyes and its active visual search. It also leads to developmental delays cognitive activity child, including a delay in the formation of his visual-spatial concepts, which are formed with the active participation of not only the above-mentioned motor, but also the visual analyzer. In the future, this can lead to specific reading and writing disorders, to difficulties in mastering such subjects as geometry, geography, drawing, drawing, etc.
  4. Often existing emotional-volitional disorders, the degree of severity and features of manifestation of which largely depend on the location and time of brain damage.
  5. Secondary mental layers associated with the child’s experience of his speech and other inferiority. With dyslalia, such layers are much less common.

It is clear that the presence of all these complex non-speech symptoms cannot but have an additional negative impact on the state of the child’s speech function and on the very course and effectiveness of correctional work with him.

Dysarthria is a speech disorder that is expressed in difficulty pronouncing certain words, individual sounds, syllables, or in their distorted pronunciation. Dysarthria occurs as a result of brain damage or a disorder of the innervation of the vocal cords, facial, respiratory muscles and muscles of the soft palate, in diseases such as cleft palate, cleft lip and due to lack of teeth.

A secondary consequence of dysarthria may be a violation of written speech, which occurs due to the inability to clearly pronounce the sounds of words. In more severe manifestations of dysarthria, speech becomes completely inaccessible to the understanding of others, which leads to limited communication and secondary signs of developmental disabilities.

Dysarthria causes

The main cause of this speech disorder is considered to be insufficient innervation of the speech apparatus, which appears as a result of damage to certain parts of the brain. In such patients, there is a limitation in the mobility of the organs involved in speech production - the tongue, palate and lips, thereby complicating articulation.

In adults, the disease can manifest itself without concomitant collapse of the speech system. Those. is not accompanied by a disorder of speech perception through hearing or a disorder of written speech. Whereas in children, dysarthria is often the cause of disorders leading to reading and writing impairments. At the same time, the speech itself is characterized by a lack of smoothness, a broken breathing rhythm, and a change in the tempo of speech in the direction of slowing down or speeding up. Depending on the degree of dysarthria and the variety of forms of manifestation, there is a classification of dysarthria. The classification of dysarthria includes the erased form of dysarthria, severe and anarthria.

The symptoms of the erased form of the disease have an erased appearance, as a result of which dysarthria is confused with a disorder such as dyslalia. Dysarthria differs from dyslalia in the presence of a focal form of neurological symptoms.

In a severe form of dysarthria, speech is characterized as inarticulate and practically incomprehensible, sound pronunciation is impaired, disorders also manifest themselves in the expressiveness of intonation, voice, and breathing.

Anarthria is accompanied by a complete lack of ability to reproduce speech.

The causes of the disease include: incompatibility of the Rh factor, toxicosis of pregnant women, various pathologies of the formation of the placenta, viral infections of the mother during pregnancy, prolonged or, conversely, rapid labor, which can cause hemorrhages in the brain, infectious diseases of the brain and its membranes in newborns.

There are severe and mild degrees of dysarthria. Severe dysarthria is inextricably linked with childhood cerebral palsy. A mild degree of dysarthria is manifested by a violation of fine motor skills, pronunciation of sounds and movements of the organs of the articulatory apparatus. At this level, speech will be understandable but unclear.

The causes of dysarthria in adults can be: stroke, vascular insufficiency, inflammation or brain tumor, degenerative, progressive and genetic diseases of the nervous system (Huntington), asthenic bulbar palsy and multiple sclerosis.

Other causes of the disease, much less common, are head injuries, poisoning carbon monoxide, drug overdose, intoxication due to excessive consumption of alcoholic beverages and drugs.

Dysarthria in children

With this disease, children experience difficulties with the articulation of speech as a whole, and not with the pronunciation of individual sounds. They also experience other disorders associated with fine and gross motor skills, difficulties with swallowing and chewing. For children with dysarthria, it is quite difficult, and sometimes completely impossible, to jump on one leg, cut out of paper with scissors, fasten buttons, and it is quite difficult for them to master written language. They often miss sounds or distort them, distorting words in the process. Sick children mostly make mistakes when using prepositions and use incorrect syntactic connections of words in sentences. Children with such disabilities should be educated in specialized institutions.

The main manifestations of dysarthria in children are impaired articulation of sounds, voice formation disorder, changes in the rhythm, intonation and tempo of speech.

The listed disorders in children vary in severity and in various combinations. This depends on the location of the focal lesion in the nervous system, the time of occurrence of such a lesion and the severity of the disorder.

Partially complicating or sometimes completely preventing articulate sound speech are disorders of phonation and articulation, which is the so-called primary defect, leading to the appearance of secondary signs that complicate its structure.

Conducted research and studies of children with this disease show that this category of children is quite heterogeneous in terms of speech, motor and mental disorders.

Classification of dysarthria and its clinical forms is based on the identification of various foci of localization of brain damage. Children suffering from various forms of the disease differ from each other in certain defects in sound pronunciation, voice, articulation, and their disorders varying degrees may be subject to correction. That is why for professional correction it is necessary to use various techniques and methods of speech therapy.

Forms of dysarthria

There are the following forms of speech dysarthria in children: bulbar, subcortical, cerebellar, cortical, erased or mild, pseudobulbar.

Bulbar dysarthria of speech is manifested by atrophy or paralysis of the muscles of the pharynx and tongue, and decreased muscle tone. With this form, speech becomes unclear, slow, and slurred. People with the bulbar form of dysarthria are characterized by weak facial activity. It appears due to tumors or inflammatory processes in the medulla oblongata. As a result of such processes, the destruction of the nuclei of the motor nerves located there occurs: the vagus, glossopharyngeal, trigeminal, facial and sublingual.

The subcortical form of dysarthria consists of impaired muscle tone and involuntary movements (hyperkinesis), which the baby is not able to control. Occurs with focal damage to the subcortical nodes of the brain. Sometimes a child cannot pronounce certain words, sounds or phrases correctly. This becomes especially relevant if the child is in a state of calm in the circle of relatives whom he trusts. However, the situation can change radically in a matter of seconds and the baby becomes unable to reproduce a single syllable. With this form of the disease, the tempo, rhythm and intonation of speech suffer. Such a baby can pronounce whole phrases very quickly or, conversely, very slowly, while making significant pauses between words. As a result of a disorder of articulation in combination with irregular voice formation and impaired speech breathing, characteristic defects in the sound-forming side of speech appear. They can manifest themselves depending on the baby’s condition and affect mainly communicative speech functions. Rarely, with this form of the disease, disturbances in the human hearing system can also be observed, which are a complication of a speech defect.

Cerebellar speech dysarthria in its pure form is quite rare. Children susceptible to this form of the disease pronounce words by chanting them, and sometimes simply shout out individual sounds.

A child with cortical dysarthria has difficulty producing sounds together when speech flows in one stream. However, at the same time, pronouncing individual words is not difficult. And the intense pace of speech leads to modifications of sounds, creating pauses between syllables and words. A fast speech rate is similar to reproducing words when you stutter.

The erased form of the disease is characterized by mild manifestations. With it, speech disorders are not identified immediately, only after a comprehensive specialized examination. Its causes are often various infectious diseases during pregnancy, fetal hypoxia, toxicosis of pregnant women, birth injuries, and infectious diseases of infants.

The pseudobulbar form of dysarthria occurs most often in children. The cause of its development may be brain damage suffered in infancy, due to birth injuries, encephalitis, intoxication, etc. With mild pseudobulbar dysarthria, speech is characterized by slowness and difficulty in pronouncing individual sounds due to disturbances in the movements of the tongue (movements are not precise enough) and lips. Moderate pseudobulbar dysarthria is characterized by a lack of facial muscle movements, limited tongue mobility, a nasal tone of voice, and profuse salivation. The severe degree of the pseudobulbar form of the disease is expressed in complete immobility of the speech apparatus, an open mouth, limited lip movement, and facial expression.

Erased dysarthria

The erased form is quite common in medicine. The main symptoms of this form of the disease are slurred and inexpressive speech, poor diction, distortion of sounds, and replacement of sounds in complex words.

The term “erased” form of dysarthria was first introduced by O. Tokareva. She describes the symptoms of this form as mild manifestations of the pseudobulbar form, which are quite difficult to overcome. Tokareva believes that children with this form of the disease can pronounce many isolated sounds as needed, but in speech they do not sufficiently differentiate sounds and poorly automate them. Pronunciation deficiencies can be completely different character. However, they are united by several common features, such as blurriness, smearing and unclear articulation, which manifest themselves especially sharply in the speech stream.

An erased form of dysarthria is a speech pathology, which is manifested by a disorder of the prosodic and phonetic components of the system, resulting from microfocal brain damage.

Today, diagnostics and methods of corrective action are rather poorly developed. This form of the disease is often diagnosed only after the child reaches the age of five. All children with suspected erased form of dysarthria are referred to a neurologist to confirm or not confirm the diagnosis. Therapy for an erased form of dysarthria should be comprehensive, combining drug treatment, psychological and pedagogical assistance and speech therapy assistance.

Symptoms of erased dysarthria: motor clumsiness, limited number of active movements, rapid muscle fatigue during functional loads. Sick children do not stand very stable on one leg and cannot jump on one leg. Such children are much later than others and have difficulty learning self-care skills, such as fastening buttons and untying a scarf. They are characterized by poor facial expressions and the inability to keep the mouth closed, since the lower jaw cannot be fixed in an elevated state. On palpation, the facial muscles are flaccid. Due to the fact that the lips are also flaccid, the necessary labialization of sounds does not occur, therefore the prosodic side of speech deteriorates. Sound pronunciation is characterized by mixing, distortion of sounds, their replacement or complete absence.

The speech of such children is quite difficult to understand; it lacks expressiveness and intelligibility. Basically, there is a defect in the reproduction of hissing and whistling sounds. Children can mix not only sounds that are close in their method of formation and complex, but also sounds that are opposite in sound. A nasal tone may appear in speech, and the tempo is often accelerated. Children have a quiet voice, they cannot change the pitch of their voice, imitating some animals. Speech is characterized by monotony.

Pseudobulbar dysarthria

Pseudobulbar dysarthria is the most common form of the disease. It is a consequence of organic brain damage suffered in early childhood. As a result of encephalitis, intoxication, tumor processes, and birth injuries in children, pseudobulbar paresis or paralysis occurs, which is caused by damage to the conductive neurons that go from the cerebral cortex to the glossopharyngeal, vagus and hypoglossal nerves. In terms of clinical symptoms in the area of ​​facial expressions and articulation, this form of the disease is similar to the bulbar form, but the likelihood of full mastery of sound pronunciation in the pseudobulbar form is significantly higher.

As a result of pseudobulbar paresis, children experience a disorder of general and speech motor skills, the sucking reflex and swallowing are impaired. The facial muscles are sluggish, and there is drooling from the mouth.

There are three degrees of severity of this form of dysarthria.

A mild degree of dysarthria is manifested by difficulty in articulation, which consists of not very accurate and slow movements of the lips and tongue. At this degree, mild, unexpressed disturbances in swallowing and chewing also occur. Due to not very clear articulation, pronunciation is impaired. Speech is characterized by slowness and blurred pronunciation of sounds. Such children most often have difficulty pronouncing letters such as: r, ch, zh, c, sh, a ringing sounds are reproduced without proper voice input.

Also difficult for children and soft sounds, which require the tongue to rise to the hard palate. Due to incorrect pronunciation, phonemic development also suffers, and written speech is impaired. But violations of the structure of the word, vocabulary, and grammatical structure are practically not observed with this form. With mild manifestations of this form of the disease, the main symptom is a violation of speech phonetics.

The average degree of pseudobulbar form is characterized by amicity and lack of facial muscle movements. Children cannot puff out their cheeks or stretch out their lips. The movements of the tongue are also limited. Children cannot lift the tip of their tongue up, turn it to the left or right and hold it in this position. It is extremely difficult to switch from one movement to another. The soft palate is also inactive, and the voice has a nasal tint.

Also characteristic signs are: excessive drooling, difficulty chewing and swallowing. As a result of violations of articulation functions, rather severe pronunciation defects appear. Speech is characterized by slurredness, slurring, and quietness. This degree of severity of the disease is manifested by unclear articulation of vowel sounds. The sounds ы, и are often mixed, and the sounds у and а are characterized by insufficient clarity. Of the consonant sounds, t, m, p, n, x, k are most often correctly pronounced. Sounds such as: ch, l, r, c are reproduced approximately. Voiced consonants are more often replaced by voiceless ones. As a result of these disorders, children's speech becomes completely unintelligible, so such children prefer to remain silent, which leads to a loss of experience in verbal communication.

A severe degree of this form of dysarthria is called anarthria and is manifested by deep muscle damage and complete immobilization of the speech apparatus. The face of sick children is mask-like, the mouth is constantly open, and the lower jaw droops. A severe degree is characterized by difficulty chewing and swallowing, a complete absence of speech, and sometimes inarticulate pronunciation of sounds.

Diagnosis of dysarthria

When diagnosing, the greatest difficulty is distinguishing dyslalia from pseudobulbar or cortical forms of dysarthria.

The erased form of dysarthria is a borderline pathology, which is on the border between dyslalia and dysarthria. All forms of dysarthria are always based on focal brain lesions with neurological microsymptoms. As a result, a special neurological examination must be performed to make a correct diagnosis.

It is also necessary to distinguish between dysarthria and aphasia. With dysarthria, speech technique is impaired, not practical functions. Those. with dysarthria, a sick child understands what is written and heard, and can logically express his thoughts, despite the defects.

A differential diagnosis is made on the basis of a general systemic examination developed by domestic speech therapists, taking into account the specifics of the listed non-speech and speech disorders, age, and psychoneurological condition of the child. How younger child and the lower his level of speech development, the more significant the analysis of non-speech disorders in diagnosis. Therefore, today, based on the assessment of non-speech disorders, methods have been developed early detection dysarthria.

The presence of pseudobulbar symptoms is the most common manifestation of dysarthria. Its first signs can be detected even in a newborn. Such symptoms are characterized by a weak cry or its absence at all, a violation of the sucking reflex, swallowing or their complete absence. The cry in sick children remains quiet for a long time, often with a nasal tint, poorly modulated.

When suckling at the breast, children may choke, turn blue, and sometimes milk may leak from the nose. In more severe cases, the child may not take the breast at all at first. Such children are fed through a tube. Breathing may be shallow, often arrhythmic and rapid. Such disorders are combined with leakage of milk from the mouth, facial asymmetry, sagging lower lip. As a result of these disorders, the baby is unable to latch onto the pacifier or nipple.

As the child grows up, the insufficiency of intonation expressiveness of the cry and vocal reactions becomes more and more apparent. All sounds made by a child are monotonous and appear later than normal. A child suffering from dysarthria cannot bite or chew for a long time, and may choke on solid food.

As the child grows up, the diagnosis is made on the basis of the following speech symptoms: persistent pronunciation defects, insufficiency of voluntary articulation, vocal reactions, incorrect placement of the tongue in the oral cavity, voice formation disorders, speech breathing and delayed speech development.

The main signs used for differential diagnosis include:

- the presence of weak articulation (insufficient bending of the tip of the tongue upward, tremor of the tongue, etc.);

— presence of prosodic disorders;

- the presence of synkinesis (for example, movements of the fingers that occur when moving the tongue);

— slowness of the tempo of articulations;

- difficulty maintaining articulation;

— difficulty in switching articulations;

- persistence of disturbances in the pronunciation of sounds and difficulty in automating the delivered sounds.

Functional tests also help to establish a correct diagnosis. For example, a speech therapist asks a child to open his mouth and stick out his tongue, which should be held motionless in the middle. At the same time, the child is shown an object moving laterally, which he needs to follow. The presence of dysarthria during this test is indicated by the movement of the tongue in the direction in which the eyes move.

When examining a child for the presence of dysarthria, it is necessary Special attention pay attention to the state of articulation at rest, during facial movements and general movements, mainly articulatory. It is necessary to pay attention to the volume of movements, their pace and smoothness of switching, proportionality and accuracy, the presence of oral synkinesis, etc.

Dysarthria treatment

The main focus of treatment for dysarthria is the development of normal speech in the child, which will be understandable to others and will not interfere with communication and further learning of basic writing and reading skills.

Correction and therapy for dysarthria must be comprehensive. In addition to constant speech therapy work, medication treatment prescribed by a neurologist and exercise therapy are also required. Therapeutic work should be aimed at treating three main syndromes: articulation and speech breathing disorders, voice disorders.

Drug therapy for dysarthria involves the prescription of nootropics (for example, Glycine, Encephabol). Their positive effect is based on the fact that they specifically affect the higher functions of the brain, stimulate mental activity, improve learning processes, intellectual activity and memory of children.

Physiotherapy exercises consist of regular special gymnastics, the effect of which is aimed at strengthening the facial muscles.

Massage has proven itself well for dysarthria, which must be done regularly and daily. In principle, massage is the first step in treating dysarthria. It consists of stroking and lightly pinching the muscles of the cheeks, lips and lower jaw, bringing the lips together with the fingers in a horizontal and vertical direction, massaging the soft palate with the pads of the index and middle fingers for no more than two minutes, and movements should be forward and backward. Massage for dysarthria is needed to normalize the tone of the muscles that take part in articulation, reduce the manifestation of paresis and hyperkinesis, activate poorly working muscles, and stimulate the formation of areas of the brain responsible for speech. The first massage should take no more than two minutes, then gradually increase the massage time until it reaches 15 minutes.

Also, to treat dysarthria, it is necessary to train respiratory system child. For this purpose, exercises developed by A. Strelnikova are often used. They involve sharp inhalations when bending over and exhalations when straightening up.

A good effect is observed with self-study. They consist in the fact that the child stands in front of a mirror and trains to reproduce the same movements of the tongue and lips that he saw when talking with others. Gymnastics techniques to improve speech: open and close your mouth, stretch your lips like a “proboscis,” hold your mouth in an open position, then in a half-open position. You need to ask the child to hold a gauze bandage between his teeth and try to pull the bandage out of his mouth. You can also use a lollipop on a shelf that the child must hold in his mouth and the adult must take it out. The smaller the lollipop, the more difficult it will be for the child to hold it.

The work of a speech therapist for dysarthria consists of automating and staging the pronunciation of sounds. You need to start with simple sounds, gradually moving on to sounds that are difficult to articulate.

Also important in the treatment and correction of dysarthria is the development of fine and gross motor skills of the hands, which are closely related to speech functions. For this purpose, finger gymnastics, assembling various puzzles and construction sets, sorting small objects and sorting them out are usually used.

The outcome of dysarthria is always ambiguous due to the fact that the disease is caused by irreversible disturbances in the functioning of the central nervous system and brain.

Correction of dysarthria

Corrective work to overcome dysarthria must be carried out regularly along with drug treatment and rehabilitation therapy (for example, treatment and preventive exercises, therapeutic baths, hirudotherapy, acupuncture, etc.), which is prescribed by a neurologist. Non-traditional correction methods have proven themselves well, such as dolphin therapy, isotherapy, touch therapy, sand therapy, etc.

Correctional classes conducted by a speech therapist imply: development of motor skills of the speech apparatus and fine motor skills, voice, formation of speech and physiological breathing, correction of incorrect sound pronunciation and consolidation of assigned sounds, work on the formation of speech communication and expressiveness of speech.

The main stages of correctional work are identified. The first stage of the lesson is a massage, with the help of which the muscle tone of the speech apparatus develops. The next step is to conduct an exercise to form correct articulation, with the goal of subsequently correctly pronouncing sounds by the child, to produce sounds. Then work is carried out on automation of sound pronunciation. The last stage is learning the correct pronunciation of words using already supplied sounds.

Equally important for a positive outcome of dysarthria is the psychological support of the child from loved ones. It is very important for parents to learn to praise their children for any of their achievements, even the smallest ones. The child must be given a positive incentive for independent study and confidence that he can do anything. If a child has no achievements at all, then you should choose a few things that he does best and praise him for them. A child should feel that he is always loved, regardless of his victories or losses, with all his shortcomings.

If a child was injured in utero or suffered a birth injury, special attention should be paid to his speech.

We continue to introduce readers to various speech disorders with the help of L. Paramonova’s book “Speech Therapy for Everyone.”

We have already talked about sound pronunciation disorders in general and dyslalia in particular. Today we will talk about dysarthria.

Dysarthria is a disorder of the sound pronunciation side of speech, which is caused by organic damage to the central part of the speech motor analyzer and the associated disruption of the innervation of the speech muscles. The term “dysarthria” itself means “disorder of articulate speech” (“artron” translated into Russian means “articulation”, and “diz” means “disorder”). The prevalence of dysarthria among mentally normal children ranges from 3 to 6%, but these figures have a clear upward trend.

Dysarthria most often is not an independent speech disorder, but is only one of the symptoms of a serious illness - cerebral palsy, which is usually congenital or occurs before the age of two years. Depending on the location of the brain lesion, dysarthria manifests itself in different ways, and therefore there are several types of it, which are inappropriate to consider here due to the impossibility of practical use of this information by non-specialists.

With complete paralysis of the articulatory muscles, anarthria occurs - a complete absence of pronunciation in the child. The main manifestations of severe dysarthria will be discussed further. But so-called erased dysarthria can often be observed, which needs to be discussed in a little more detail, since it is very widespread and, moreover, can be difficult to distinguish from dyslalia.

Erased dysarthria

Erased dysarthria is based on very small, literally pinpoint organic lesions of the cerebral cortex. Their presence leads to paresis of only certain small groups of articulatory muscles (for example, only the tip of the tongue or only one side of it). Under such conditions, the child suffers from the pronunciation of only individual sounds at an almost normal rate and rhythm of speech and in the absence of pronounced disorders of speech breathing and voice.

For a long time, such disorders in the pronunciation of sounds were classified as functional motor dyslalia, without noticing their specificity. However, the difficulties of overcoming them forced specialists to study this issue more carefully, as a result of which erased dysarthria was separated from the group of functional motor dyslalia. (During a neurological examination, paresis of individual articulatory muscles was discovered in these children, leading to definite disturbances in the pronunciation of sounds.)

Sound pronunciation disorders with erased dysarthria have not only a different causality compared to dyslalia, but also a different external manifestation. In particular, erased dysarthria is characterized by interdental pronunciation of sounds associated with weakness (pareticity) of the muscles of the tip of the tongue - it simply cannot be held behind the teeth. Often there is a “lateral” pronunciation of some consonants, which is associated with paresis of one side of the tongue. In these cases, the tongue, when protruding from the mouth, usually deviates to one side, and when articulating some sounds it becomes an “edge” in the mouth, which contributes to lateral air leakage. Such disturbances in the pronunciation of sounds at any age cannot be attributed to age-related peculiarities of sound pronunciation due to their being due to pathological reasons. Erased dysarthria never goes away with age, as evidenced by its presence in many adults.

Causes of cerebral palsy and dysarthria

The causes of cerebral palsy, and therefore the causes of dysarthria, are organic lesions of the child’s nervous system, which can occur in utero, during childbirth or as a result of early childhood diseases (meningitis, meningoencephalitis, traumatic lesions or vascular disorders).

Until relatively recently, the main cause of cerebral palsy (and therefore dysarthria) was considered to be birth trauma, causing cerebral hemorrhage, birth asphyxia and other complications during childbirth. However, it has now become clear that in more than 80-90% of cases, damage to the fetal nervous system occurs in utero. It is the insufficient usefulness of the fetus and its “unpreparedness” for active participation in the process of childbirth that leads to its complicated course and possible additional brain damage. These injuries can be the result of cesarean section, asphyxia at birth, or birth trauma during the provision of mechanical assistance, which is a forced means and is used only in cases of extreme necessity. Knowledge of this circumstance is extremely important both from the point of view of preventing cerebral palsy and, in most cases, the dysarthria that accompanies it.

If the main reason for the occurrence of both is not “for some unknown reason” that labor is so difficult, then the main content of prevention should be concern for the normal course of pregnancy, which very much depends on the seriousness of the woman’s attitude towards this most important period of her life. It has complete power to exclude such pathogenic factors, which are harmful to the intrauterine development of the fetus, but, nevertheless, are often present, such as smoking and drinking alcoholic beverages even during pregnancy, constant overwork and non-compliance with a healthy daily routine, and continued work in hazardous industries. and on the night shift, heavy lifting and generally heavy physical exertion, “emergency” flights and transfers to other cities or even to other continents almost before the birth itself, which in such cases often begins right on the road and therefore, in principle, cannot proceed Fine.

Speech and non-speech symptoms of dysarthria

Speech symptoms. The speech of children suffering from a severe form of dysarthria actually loses its articulation and becomes almost incomprehensible to others (“like porridge in the mouth”). What's the matter here? As previously noted, motor commands from the central part of the speech motor analyzer to the peripheral speech organs are transmitted along nerve pathways. With organic damage to these speech parts of the brain or directly to the motor nerves, full transmission of nerve impulses becomes impossible, and phenomena of paralysis or paresis develop in the muscles themselves. And since these paresis can spread not only to the muscles of the tongue and lips, but also to the muscles of the soft palate, vocal cords and respiratory organs, with dysarthria not only the articulation of sounds is impaired, but also voice formation and speech breathing.

With severe paresis of the tongue, the articulation of almost all speech sounds, including vowels, suffers. Paresis of the soft palate causes the appearance of a nasal tone of the voice, paresis of the vocal cords - a violation of the process of voice formation and a change in the timbre of the voice, paresis of the respiratory muscles - a violation of the function of speech breathing, which becomes superficial and arrhythmic, and therefore does not provide a full air stream for voice formation.

In addition to impaired motor function of the speech muscles due to the presence of paralysis and paresis, the sensitivity of these muscles also suffers, and therefore the child does not feel the position of his articulatory organs well enough. For this reason, it is difficult for him to find the necessary articulations, which creates additional difficulties both in mastering sound pronunciation and in correcting it.

All this taken together leads to the fact that dysarthria, in its external manifestations, differs sharply from dyslalia. So, if with dyslalia (with the exception of mechanical dyslalia due to congenital cleft palates) defects in sound pronunciation appear against the background of normal tempo and rhythm of speech, normal speech breathing and voice formation, then with dysarthria there is a picture of a general phonetic disadvantage of speech as a whole, as a result of which it loses its intelligibility, articulation.

Constantly hearing a child's own slurred speech in many cases leads to the appearance of secondary disorders of auditory differentiation of sounds.

The imperfection of auditory differentiation of sounds, in turn, secondarily causes difficulties in mastering the phonemic analysis of words.

Poor orientation in the sound composition of speech, associated with impaired auditory differentiation of sounds and difficulties in phonemic analysis of words, inevitably leads to the appearance of specific writing disorders in children - corresponding types of dysgraphia.

The difficulty and insufficiency of verbal communication may also be secondary to the poverty of the child’s vocabulary and the unformed grammatical structure of his speech.

Thus, with severe dysarthria, speech suffers primarily or secondarily, in fact, in all its links, and not just in relation to sound pronunciation itself.

Non-speech symptoms. Dysarthria against the background of cerebral palsy is characterized by the presence of not only the speech symptoms discussed above, but also a number of non-speech symptoms, which ultimately also, in one way or another, make it difficult to master speech. These symptoms include the following.

  1. Paralysis and paresis of the muscles of the limbs and torso. Paresis of the legs sharply limits (or even completely eliminates) the child’s ability to move in space, which disrupts the development of his visual-spatial concepts, since he perceives space by the measure of his own steps. Otherwise, he cannot even judge the degree of distance from him of certain objects, so it is not by chance that a child who has not yet mastered the skill of walking tries to reach the moon from the sky, stretching out his little hand to it - it seems to him that it is very close.

Paralysis and paresis of the hands limit (or exclude) the possibility of manipulating objects, which in the second year of a child’s life plays a decisive role in his knowledge of the world around him (the activity of the “cognitive hand”). Holding various toys in his hands, and also often bringing them to his mouth and trying to lick and even “taste” them, the child gradually gets an idea of ​​their shape, size, smoothness or roughness of the surface, temperature, which is different for cold metal objects and much warmer wooden ones. and plush, etc.

It is quite understandable that if in his sensory experience a child has not received an idea of ​​the spatial and other characteristics of objects, then he will also have difficulty in verbally denoting these characteristics. It will be very difficult for him not only to express in words what is further and what is closer, which object is higher and which is lower, etc., but even to understand these spatial relationships between objects.

  • Frequently observed paresis of the extraocular muscles. With paresis of these muscles, the child is impaired in such important visual functions as fixing the gaze on an object, “feeling” it with the gaze, “tracing” a moving object with the eyes and its active visual search. This also leads to a delay in the development of the child’s cognitive activity, including a delay in the formation of his visual-spatial concepts, which are formed with the active participation of not only the above-mentioned motor, but also the visual analyzer. In the future, this can lead to specific reading and writing disorders, to difficulties in mastering such subjects as geometry, geography, drawing, drawing, etc.
  • Often there are emotional-volitional disorders, the degree of severity and features of manifestation of which largely depend on the location and time of brain damage.
  • Secondary mental layers associated with the child’s experience of his speech and other inferiority. With dyslalia, such layers are much less common.
  • It is clear that the presence of all these complex non-speech symptoms cannot but have an additional negative impact on the state of the child’s speech function and on the very course and effectiveness of correctional work with him.

    Dysarthria

    Dysarthria is a disorder of the pronunciation organization of speech associated with damage to the central part of the speech motor analyzer and a violation of the innervation of the muscles of the articulatory apparatus. The structure of the defect in dysarthria includes violations of speech motor skills, sound pronunciation, speech breathing, voice and prosodic aspects of speech; with severe lesions, anarthria occurs. If dysarthria is suspected, neurological diagnostics (EEG, EMG, ENG, MRI of the brain, etc.) and speech therapy examination of oral and written speech are performed. Corrective work for dysarthria includes therapeutic interventions (medication courses, exercise therapy, massage, physical therapy), speech therapy classes, articulation gymnastics, speech therapy massage.

    Dysarthria

    Dysarthria is a severe speech disorder, accompanied by a disorder of articulation, phonation, speech breathing, tempo-rhythmic organization and intonation coloring of speech, as a result of which speech loses its articulation and intelligibility. Among children, the prevalence of dysarthria is 3-6%, but in recent years there has been a pronounced upward trend in this speech pathology. In speech therapy, dysarthria is one of the three most common forms of oral speech disorders, second only to dyslalia in frequency and ahead of alalia. Since the pathogenesis of dysarthria is based on organic lesions of the central and peripheral nervous system, this speech disorder is also studied by specialists in the field of neurology and psychiatry.

    Causes of dysarthria

    Most often (in 65-85% of cases) dysarthria accompanies cerebral palsy and has the same causes. In this case, organic damage to the central nervous system occurs in the prenatal, birth or early periods of child development (usually up to 2 years). The most common perinatal factors of dysarthria are toxicosis of pregnancy, fetal hypoxia, Rhesus conflict, chronic somatic diseases of the mother, pathological course of labor, birth injuries, birth asphyxia, kernicterus of newborns, prematurity, etc. The severity of dysarthria is closely related to the severity of motor disorders during Cerebral palsy: for example, with double hemiplegia, dysarthria or anarthria is detected in almost all children.

    In early childhood, damage to the central nervous system and dysarthria in a child can develop after suffering neuroinfections (meningitis, encephalitis), purulent otitis media, hydrocephalus, traumatic brain injury, severe intoxication.

    Classification of dysarthria

    The neurological classification of dysarthria is based on the principle of localization and a syndromic approach. Taking into account the localization of damage to the speech-motor apparatus, the following are distinguished:

    • bulbar dysarthria associated with damage to the nuclei of the cranial nerves (glossopharyngeal, sublingual, vagus, sometimes facial, trigeminal) in the medulla oblongata
    • pseudobulbar dysarthria associated with damage to the corticonuclear pathways
    • extrapyramidal (subcortical) dysarthria associated with damage to the subcortical nuclei of the brain
    • cerebellar dysarthria associated with damage to the cerebellum and its pathways
    • cortical dysarthria associated with focal lesions of the cerebral cortex.

    Depending on the leading clinical syndrome, cerebral palsy may include spastic-rigid, spastic-paretic, spastic-hyperkinetic, spastic-atactic, ataxic-hyperkinetic dysarthria.

    Speech therapy classification is based on the principle of speech intelligibility for others and includes 4 degrees of severity of dysarthria:

    1st degree (erased dysarthria) – defects in sound pronunciation can only be identified by a speech therapist during a special examination.

    2nd degree - defects in sound pronunciation are noticeable to others, but overall speech remains understandable.

    3rd degree - understanding of the speech of a patient with dysarthria is available only to those close to him and partially to strangers.

    4th degree – speech is absent or incomprehensible even to the closest people (anarthria).

    Symptoms of dysarthria

    The speech of patients with dysarthria is slurred, unclear, and incomprehensible (“porridge in the mouth”), which is due to insufficient innervation of the muscles of the lips, tongue, soft palate, vocal folds, larynx, and respiratory muscles. Therefore, with dysarthria, a whole complex of speech and non-speech disorders develops, which constitute the essence of the defect.

    Impaired articulatory motor skills in patients with dysarthria may manifest as spasticity, hypotonia, or dystonia of the articulatory muscles. Muscle spasticity is accompanied by constant increased tone and tension in the muscles of the lips, tongue, face, and neck; tightly closed lips, limiting articulatory movements. With muscle hypotonia, the tongue is flaccid and lies motionless on the floor of the mouth; the lips do not close, the mouth is half open, hypersalivation (salivation) is pronounced; Due to paresis of the soft palate, a nasal tone of voice appears (nasalization). In the case of dysarthria occurring with muscular dystonia, when attempting to speak, muscle tone changes from low to increased.

    Sound pronunciation disturbances in dysarthria can be expressed to varying degrees, depending on the location and severity of damage to the nervous system. With erased dysarthria, individual phonetic defects (sound distortions) and “blurred” speech are observed.” With more pronounced degrees of dysarthria, there are distortions, omissions, and substitutions of sounds; speech becomes slow, inexpressive, slurred. General speech activity is noticeably reduced. In the most severe cases, with complete paralysis of the speech motor muscles, motor speech becomes impossible.

    Specific features of impaired sound pronunciation in dysarthria are the persistence of defects and the difficulty of overcoming them, as well as the need for a longer period of automation of sounds. With dysarthria, the articulation of almost all speech sounds, including vowels, is impaired. Dysarthria is characterized by interdental and lateral pronunciation of hissing and whistling sounds; voicing defects, palatalization (softening) of hard consonants.

    Due to insufficient innervation of the speech muscles during dysarthria, speech breathing is disrupted: exhalation is shortened, breathing at the time of speech becomes rapid and intermittent. Voice disturbances in dysarthria are characterized by insufficient strength (quiet, weak, fading voice), changes in timbre (deafness, nasalization), and melodic-intonation disorders (monotony, absence or inexpressibility of voice modulations).

    Due to slurred speech in children with dysarthria, auditory differentiation of sounds and phonemic analysis and synthesis suffer secondarily. The difficulty and insufficiency of verbal communication can lead to an undeveloped vocabulary and grammatical structure of speech. Therefore, children with dysarthria may experience phonetic-phonemic (FFN) or general speech underdevelopment (GSD) and associated corresponding types of dysgraphia.

    Characteristics of clinical forms of dysarthria

    Bulbar dysarthria is characterized by areflexia, amymia, disorder of sucking, swallowing solid and liquid food, chewing, hypersalivation caused by atony of the muscles of the oral cavity. The articulation of sounds is slurred and extremely simplified. All the variety of consonants is reduced into a single fricative sound; sounds are not differentiated from each other. Nasalization of voice timbre, dysphonia or aphonia is typical.

    With pseudobulbar dysarthria, the nature of the disorder is determined by spastic paralysis and muscle hypertonicity. Pseudobulbar paralysis manifests itself most clearly in impaired tongue movements: great difficulty is caused by attempts to raise the tip of the tongue upward, move it to the sides, or hold it in a certain position. With pseudobulbar dysarthria, switching from one articulatory posture to another is difficult. Typically selective impairment of voluntary movements, synkinesis (conjugal movements); profuse salivation, increased pharyngeal reflex, choking, dysphagia. The speech of patients with pseudobulbar dysarthria is blurred, slurred, and has a nasal tint; the normative reproduction of sonors, whistling and hissing, is grossly violated.

    Subcortical dysarthria is characterized by the presence of hyperkinesis - involuntary violent muscle movements, including facial and articulatory ones. Hyperkinesis can occur at rest, but usually intensifies when attempting to speak, causing articulatory spasm. There is a violation of the timbre and strength of the voice, the prosodic aspect of speech; Sometimes patients emit involuntary guttural screams.

    With subcortical dysarthria, the tempo of speech may be disrupted, such as bradylalia, tachylalia, or speech dysrhythmia (organic stuttering). Subcortical dysarthria is often combined with pseudobulbar, bulbar and cerebellar forms.

    A typical manifestation of cerebellar dysarthria is a violation of the coordination of the speech process, which results in tremor of the tongue, jerky, scanned speech, and occasional cries. Speech is slow and slurred; The pronunciation of front-lingual and labial sounds is most affected. With cerebellar dysarthria, ataxia is observed (unsteadiness of gait, imbalance, clumsiness of movements).

    Cortical dysarthria in its speech manifestations resembles motor aphasia and is characterized by a violation of voluntary articulatory motor skills. There are no disorders of speech breathing, voice, or prosody in cortical dysarthria. Taking into account the localization of lesions, kinesthetic postcentral cortical dysarthria (afferent cortical dysarthria) and kinetic premotor cortical dysarthria (efferent cortical dysarthria) are distinguished. However, with cortical dysarthria there is only articulatory apraxia, while with motor aphasia not only the articulation of sounds suffers, but also reading, writing, understanding speech, and using language.

    Diagnosis of dysarthria

    The examination and subsequent management of patients with dysarthria is carried out by a neurologist (children's neurologist) and speech therapist. The extent of the neurological examination depends on the expected clinical diagnosis. The most important diagnostic value is given by electrophysiological studies (electroencephalography, electromyography, electroneurography), transcranial magnetic stimulation, MRI of the brain, etc.

    Speech therapy examination for dysarthria includes assessment of speech and non-speech disorders. Assessment of non-speech symptoms involves studying the structure of the articulatory apparatus, the volume of articulatory movements, the state of facial and speech muscles, and the nature of breathing. The speech therapist pays special attention to the history of speech development. As part of the diagnosis of oral speech in dysarthria, a study of the pronunciation aspect of speech (sound pronunciation, tempo, rhythm, prosody, speech intelligibility) is carried out; synchronicity of articulation, breathing and voice production; phonemic perception, level of development of the lexico-grammatical structure of speech. In the process of diagnosing written speech, tasks are given for copying text and writing from dictation, reading passages and comprehending what is read.

    Based on the examination results, it is necessary to distinguish between dysarthria and motor alalia, motor aphasia, and dyslalia.

    Correction of dysarthria

    Speech therapy work to overcome dysarthria should be carried out systematically, against the background of drug therapy and rehabilitation (segmental reflex and acupressure, acupressure, exercise therapy, therapeutic baths, physiotherapy, mechanotherapy, acupuncture, hirudotherapy), prescribed by a neurologist. A good background for correctional and pedagogical classes is achieved by using non-traditional forms of restorative treatment: dolphin therapy, touch therapy, isotherapy, sand therapy, etc.

    On speech therapy classes to correct dysarthria, the development of fine motor skills (finger gymnastics), motor skills of the speech apparatus (speech therapy massage, articulation gymnastics) is carried out; physiological and speech breathing (breathing exercises), voice (orthophonic exercises); correction of impaired and consolidation of correct sound pronunciation; work on the expressiveness of speech and the development of verbal communication.

    The order of production and automation of sounds is determined by the greatest availability of articulation patterns at the moment. Automation of sounds in dysarthria is sometimes carried out until complete purity of their isolated pronunciation is achieved, and the process itself requires more time and persistence than in dyslalia.

    Forecast and prevention of dysarthria

    Only early, systematic speech therapy work to correct dysarthria can give positive results. A major role in the success of correctional pedagogical intervention is played by the therapy of the underlying disease, the diligence of the dysarthric patient himself and his close circle.

    Under these conditions, one can count on almost complete normalization of speech function in the case of erased dysarthria. Having mastered the skills of correct speech, such children can successfully study in a comprehensive school, and receive the necessary speech therapy help in clinics or at school speech centers.

    At severe forms dysarthria, it is only possible to improve the state of speech function. The continuity of various types of speech therapy institutions is important for the socialization and education of children with dysarthria: kindergartens and schools for children with severe speech disorders, speech departments of psychoneurological hospitals; friendly work of a speech therapist, neurologist, psychoneurologist, massage therapist, and physical therapy specialist.

    Medical and pedagogical work to prevent dysarthria in children with perinatal brain damage should begin from the first months of life. Prevention of dysarthria in early childhood and adulthood involves preventing neuroinfections, brain injuries, and toxic effects.

    Tongue paresis in children

    Paresis of the muscles of the tongue and oropharynx leads to impaired swallowing, phonation and articulation, as well as the inability to whistle.

    Variable severity of paresis:

    It increases in the evening, as well as when the affected muscles are stressed - during a long conversation or when eating. No muscle atrophy is observed. Symptoms appeared several weeks or months ago, and their severity varies. We are talking about myasthenia gravis, less often about a space-occupying process that compresses the brain stem.

    If an elderly person develops masticatory paresis while chewing and is accompanied by pain, this raises the suspicion of “intermittent claudication of the masticatory muscles” associated with giant cell arteritis or other vasculitis.

    Articulation disturbances may be intermittent in nature during paroxysmal dysarthria, for example, as part of multiple sclerosis. However, it is not a sign of true paresis of the laryngeal muscles and is accompanied by a history and objective symptoms characteristic of multiple sclerosis.

    The severity of paresis is constant:

    Paresis and swelling of the masticatory muscles, which is sometimes accompanied by pain, may be a sign of a tumor, as well as localized myositis with spontaneous recovery. These two reasons can only be distinguished by using histological examination. With benign myositis, damage to other muscles of the head and face is sometimes associated.

    Bilateral tongue atrophy and fasciculations are detected (which are better visible if the tongue is inside the oral cavity). In most cases, fasciculations, as well as paresis and atrophy, are observed in other muscles. We are talking about bulbar palsy in amyotrophic lateral sclerosis.

    When collecting anamnesis, it turns out that the disorder slowly progresses over several months. Differential diagnosis in such cases is carried out with space-occupying processes near the brain stem, in particular, meningiomas of the foramen magnum region. If hearing loss occurs, this raises suspicion of a rare disease - Brown-Vialetto-van Laere syndrome.

    Exclusively bilateral paresis of the tongue, in the absence of fasciculation and signs of damage to other muscles of the oropharynx, indicates a bilateral lesion of the hypoglossal nerve, for example, with cranial polyradiculopathy. Atrophy of the tongue becomes noticeable only three weeks or more after the onset of the disease. There are no atrophies or fasciculations in the affected muscles.

    Perioral and nasopalpebral reflexes are animated, bilateral pyramidal signs are revealed on the extremities, and walking with small steps is characteristic. Patients are mostly elderly and/or have vascular risk factors. Paresis progresses slowly over many months or develops acutely after a hemispheric stroke: we are talking about pseudobulbar palsy due to bilateral damage to the central motor neuron, especially the corticobulbar tracts.

    Unilateral paresis of the tongue muscles is a sign of damage to the hypoglossal nerve or the region of its nuclei. With peripheral damage, taste disturbances may also occur. The cause may be a glomus tumor or carotid artery dissection. With a nuclear lesion, signs of dysfunction of the brain stem are always associated, and fasciculations are also possible.

    Paresis of the pharyngeal muscles may result from:

    Lesions of the wandering and glossopharyngeal nerves. Unilateral paresis is characteristic of peripheral damage to the nerve trunks, for example, in the opening of the jugular vein, and in this case is one of the elements of Siebenmann syndrome; unilateral nuclear damage develops as part of the Avellis, Tapia and Vernet syndromes with a trunk stroke,

    Bilateral paresis raises suspicions of diphtheria, cranial polyradiculopathy, or, if the severity of paresis is variable, myasthenia gravis.

    Tongue paresis in children

    Dysarthria is a speech disorder that is expressed in difficulty pronouncing certain words, individual sounds, syllables, or in their distorted pronunciation. Dysarthria occurs as a result of brain damage or a disorder of the innervation of the vocal cords, facial, respiratory muscles and muscles of the soft palate, in diseases such as cleft palate, cleft lip and due to lack of teeth.

    A secondary consequence of dysarthria may be a violation of written speech, which occurs due to the inability to clearly pronounce the sounds of words. In more severe manifestations of dysarthria, speech becomes completely inaccessible to the understanding of others, which leads to limited communication and secondary signs of developmental disabilities.

    Dysarthria causes

    The main cause of this speech disorder is considered to be insufficient innervation of the speech apparatus, which appears as a result of damage to certain parts of the brain. In such patients, there is a limitation in the mobility of the organs involved in speech production - the tongue, palate and lips, thereby complicating articulation.

    In adults, the disease can manifest itself without concomitant collapse of the speech system. Those. is not accompanied by a disorder of speech perception through hearing or a disorder of written speech. Whereas in children, dysarthria is often the cause of disorders leading to reading and writing impairments. At the same time, the speech itself is characterized by a lack of smoothness, a broken breathing rhythm, and a change in the tempo of speech in the direction of slowing down or speeding up. Depending on the degree of dysarthria and the variety of forms of manifestation, there is a classification of dysarthria. The classification of dysarthria includes the erased form of dysarthria, severe and anarthria.

    The symptoms of the erased form of the disease have an erased appearance, as a result of which dysarthria is confused with a disorder such as dyslalia. Dysarthria differs from dyslalia in the presence of a focal form of neurological symptoms.

    In a severe form of dysarthria, speech is characterized as inarticulate and practically incomprehensible, sound pronunciation is impaired, disorders also manifest themselves in the expressiveness of intonation, voice, and breathing.

    Anarthria is accompanied by a complete lack of ability to reproduce speech.

    The causes of the disease include: incompatibility of the Rh factor, toxicosis of pregnant women, various pathologies of the formation of the placenta, viral infections of the mother during pregnancy, prolonged or, conversely, rapid labor, which can cause hemorrhages in the brain, infectious diseases of the brain and its membranes in newborns.

    There are severe and mild degrees of dysarthria. Severe dysarthria is inextricably linked with cerebral palsy. A mild degree of dysarthria is manifested by a violation of fine motor skills, pronunciation of sounds and movements of the organs of the articulatory apparatus. At this level, speech will be understandable but unclear.

    The causes of dysarthria in adults can be: stroke, vascular insufficiency, inflammation or brain tumor, degenerative, progressive and genetic diseases of the nervous system (Alzheimer's, Huntington's disease), asthenic bulbar palsy and multiple sclerosis.

    Other causes of the disease, much less common, are head injuries, carbon monoxide poisoning, drug overdose, and intoxication due to excessive consumption of alcoholic beverages and drugs.

    Dysarthria in children

    With this disease, children experience difficulties with the articulation of speech as a whole, and not with the pronunciation of individual sounds. They also experience other disorders associated with fine and gross motor skills, difficulties with swallowing and chewing. For children with dysarthria, it is quite difficult, and sometimes completely impossible, to jump on one leg, cut out of paper with scissors, fasten buttons, and it is quite difficult for them to master written language. They often miss sounds or distort them, distorting words in the process. Sick children mostly make mistakes when using prepositions and use incorrect syntactic connections of words in sentences. Children with such disabilities should be educated in specialized institutions.

    The main manifestations of dysarthria in children are impaired articulation of sounds, voice formation disorder, changes in the rhythm, intonation and tempo of speech.

    The listed disorders in children vary in severity and in various combinations. This depends on the location of the focal lesion in the nervous system, the time of occurrence of such a lesion and the severity of the disorder.

    Partially complicating or sometimes completely preventing articulate sound speech are disorders of phonation and articulation, which is the so-called primary defect, leading to the appearance of secondary signs that complicate its structure.

    Conducted research and studies of children with this disease show that this category of children is quite heterogeneous in terms of speech, motor and mental disorders.

    The classification of dysarthria and its clinical forms is based on the identification of various foci of localization of brain damage. Children suffering from various forms of the disease differ from each other in certain defects in sound pronunciation, voice, articulation; their disorders of varying degrees can be corrected. That is why for professional correction it is necessary to use various techniques and methods of speech therapy.

    Forms of dysarthria

    There are the following forms of speech dysarthria in children: bulbar, subcortical, cerebellar, cortical, erased or mild, pseudobulbar.

    Bulbar dysarthria of speech is manifested by atrophy or paralysis of the muscles of the pharynx and tongue, and decreased muscle tone. With this form, speech becomes unclear, slow, and slurred. People with the bulbar form of dysarthria are characterized by weak facial activity. It appears due to tumors or inflammatory processes in the medulla oblongata. As a result of such processes, the destruction of the nuclei of the motor nerves located there occurs: the vagus, glossopharyngeal, trigeminal, facial and sublingual.

    The subcortical form of dysarthria consists of impaired muscle tone and involuntary movements (hyperkinesis), which the baby is not able to control. Occurs with focal damage to the subcortical nodes of the brain. Sometimes a child cannot pronounce certain words, sounds or phrases correctly. This becomes especially relevant if the child is in a state of calm in the circle of relatives whom he trusts. However, the situation can change radically in a matter of seconds and the baby becomes unable to reproduce a single syllable. With this form of the disease, the tempo, rhythm and intonation of speech suffer. Such a baby can pronounce whole phrases very quickly or, conversely, very slowly, while making significant pauses between words. As a result of a disorder of articulation in combination with irregular voice formation and impaired speech breathing, characteristic defects in the sound-forming side of speech appear. They can manifest themselves depending on the baby’s condition and affect mainly communicative speech functions. Rarely, with this form of the disease, disturbances in the human hearing system can also be observed, which are a complication of a speech defect.

    Cerebellar speech dysarthria in its pure form is quite rare. Children susceptible to this form of the disease pronounce words by chanting them, and sometimes simply shout out individual sounds.

    A child with cortical dysarthria has difficulty producing sounds together when speech flows in one stream. However, at the same time, pronouncing individual words is not difficult. And the intense pace of speech leads to modifications of sounds, creating pauses between syllables and words. A fast speech rate is similar to reproducing words when you stutter.

    The erased form of the disease is characterized by mild manifestations. With it, speech disorders are not identified immediately, only after a comprehensive specialized examination. Its causes are often various infectious diseases during pregnancy, fetal hypoxia, toxicosis of pregnant women, birth injuries, and infectious diseases of infants.

    The pseudobulbar form of dysarthria occurs most often in children. The cause of its development may be brain damage suffered in infancy, due to birth injuries, encephalitis, intoxication, etc. With mild pseudobulbar dysarthria, speech is characterized by slowness and difficulty in pronouncing individual sounds due to disturbances in the movements of the tongue (movements are not precise enough) and lips. Moderate pseudobulbar dysarthria is characterized by a lack of facial muscle movements, limited tongue mobility, a nasal tone of voice, and profuse salivation. The severe degree of the pseudobulbar form of the disease is expressed in complete immobility of the speech apparatus, an open mouth, limited lip movement, and facial expression.

    Erased dysarthria

    The erased form is quite common in medicine. The main symptoms of this form of the disease are slurred and inexpressive speech, poor diction, distortion of sounds, and replacement of sounds in complex words.

    The term “erased” form of dysarthria was first introduced by O. Tokareva. She describes the symptoms of this form as mild manifestations of the pseudobulbar form, which are quite difficult to overcome. Tokareva believes that children with this form of the disease can pronounce many isolated sounds as needed, but in speech they do not sufficiently differentiate sounds and poorly automate them. Pronunciation deficiencies can be of a completely different nature. However, they are united by several common features, such as blurriness, smearing and unclear articulation, which manifest themselves especially sharply in the speech stream.

    An erased form of dysarthria is a speech pathology, which is manifested by a disorder of the prosodic and phonetic components of the system, resulting from microfocal brain damage.

    Today, diagnostics and methods of corrective action are rather poorly developed. This form of the disease is often diagnosed only after the child reaches the age of five. All children with suspected erased form of dysarthria are referred to a neurologist to confirm or not confirm the diagnosis. Therapy for an erased form of dysarthria should be comprehensive, combining drug treatment, psychological and pedagogical assistance and speech therapy assistance.

    Symptoms of erased dysarthria: motor clumsiness, limited number of active movements, rapid muscle fatigue during functional loads. Sick children do not stand very stable on one leg and cannot jump on one leg. Such children are much later than others and have difficulty learning self-care skills, such as fastening buttons and untying a scarf. They are characterized by poor facial expressions and the inability to keep the mouth closed, since the lower jaw cannot be fixed in an elevated state. On palpation, the facial muscles are flaccid. Due to the fact that the lips are also flaccid, the necessary labialization of sounds does not occur, therefore the prosodic side of speech deteriorates. Sound pronunciation is characterized by mixing, distortion of sounds, their replacement or complete absence.

    The speech of such children is quite difficult to understand; it lacks expressiveness and intelligibility. Basically, there is a defect in the reproduction of hissing and whistling sounds. Children can mix not only sounds that are close in their method of formation and complex, but also sounds that are opposite in sound. A nasal tone may appear in speech, and the tempo is often accelerated. Children have a quiet voice, they cannot change the pitch of their voice, imitating some animals. Speech is characterized by monotony.

    Pseudobulbar dysarthria

    Pseudobulbar dysarthria is the most common form of the disease. It is a consequence of organic brain damage suffered in early childhood. As a result of encephalitis, intoxication, tumor processes, and birth injuries in children, pseudobulbar paresis or paralysis occurs, which is caused by damage to the conductive neurons that go from the cerebral cortex to the glossopharyngeal, vagus and hypoglossal nerves. In terms of clinical symptoms in the area of ​​facial expressions and articulation, this form of the disease is similar to the bulbar form, but the likelihood of full mastery of sound pronunciation in the pseudobulbar form is significantly higher.

    As a result of pseudobulbar paresis, children experience a disorder of general and speech motor skills, the sucking reflex and swallowing are impaired. The facial muscles are sluggish, and there is drooling from the mouth.

    There are three degrees of severity of this form of dysarthria.

    A mild degree of dysarthria is manifested by difficulty in articulation, which consists of not very accurate and slow movements of the lips and tongue. At this degree, mild, unexpressed disturbances in swallowing and chewing also occur. Due to not very clear articulation, pronunciation is impaired. Speech is characterized by slowness and blurred pronunciation of sounds. Such children most often have difficulty pronouncing letters such as: r, ch, zh, ts, sh, and voiced sounds are reproduced without proper participation of the voice.

    Also difficult for children are soft sounds that require raising the tongue to the hard palate. Due to incorrect pronunciation, phonemic development also suffers, and written speech is impaired. But violations of the structure of the word, vocabulary, and grammatical structure are practically not observed with this form. With mild manifestations of this form of the disease, the main symptom is a violation of speech phonetics.

    The average degree of pseudobulbar form is characterized by amicity and lack of facial muscle movements. Children cannot puff out their cheeks or stretch out their lips. The movements of the tongue are also limited. Children cannot lift the tip of their tongue up, turn it to the left or right and hold it in this position. It is extremely difficult to switch from one movement to another. The soft palate is also inactive, and the voice has a nasal tint.

    Also characteristic signs are: excessive drooling, difficulty chewing and swallowing. As a result of violations of articulation functions, rather severe pronunciation defects appear. Speech is characterized by slurredness, slurring, and quietness. This degree of severity of the disease is manifested by unclear articulation of vowel sounds. The sounds ы, и are often mixed, and the sounds у and а are characterized by insufficient clarity. Of the consonant sounds, t, m, p, n, x, k are most often correctly pronounced. Sounds such as: ch, l, r, c are reproduced approximately. Voiced consonants are more often replaced by voiceless ones. As a result of these disorders, children's speech becomes completely unintelligible, so such children prefer to remain silent, which leads to a loss of experience in verbal communication.

    A severe degree of this form of dysarthria is called anarthria and is manifested by deep muscle damage and complete immobilization of the speech apparatus. The face of sick children is mask-like, the mouth is constantly open, and the lower jaw droops. A severe degree is characterized by difficulty chewing and swallowing, a complete absence of speech, and sometimes inarticulate pronunciation of sounds.

    Diagnosis of dysarthria

    When diagnosing, the greatest difficulty is distinguishing dyslalia from pseudobulbar or cortical forms of dysarthria.

    The erased form of dysarthria is a borderline pathology, which is on the border between dyslalia and dysarthria. All forms of dysarthria are always based on focal brain lesions with neurological microsymptoms. As a result, a special neurological examination must be performed to make a correct diagnosis.

    It is also necessary to distinguish between dysarthria and aphasia. With dysarthria, speech technique is impaired, not practical functions. Those. with dysarthria, a sick child understands what is written and heard, and can logically express his thoughts, despite the defects.

    A differential diagnosis is made on the basis of a general systemic examination developed by domestic speech therapists, taking into account the specifics of the listed non-speech and speech disorders, age, and psychoneurological condition of the child. The younger the child and the lower his level of speech development, the more important the analysis of non-speech disorders in diagnosis. Therefore, today, based on the assessment of non-speech disorders, methods for the early detection of dysarthria have been developed.

    The presence of pseudobulbar symptoms is the most common manifestation of dysarthria. Its first signs can be detected even in a newborn. Such symptoms are characterized by a weak cry or its absence at all, a violation of the sucking reflex, swallowing or their complete absence. The cry in sick children remains quiet for a long time, often with a nasal tint, poorly modulated.

    When suckling at the breast, children may choke, turn blue, and sometimes milk may leak from the nose. In more severe cases, the child may not take the breast at all at first. Such children are fed through a tube. Breathing may be shallow, often arrhythmic and rapid. Such disorders are combined with leakage of milk from the mouth, facial asymmetry, and sagging lower lip. As a result of these disorders, the baby is unable to latch onto the pacifier or nipple.

    As the child grows up, the insufficiency of intonation expressiveness of the cry and vocal reactions becomes more and more apparent. All sounds made by a child are monotonous and appear later than normal. A child suffering from dysarthria cannot bite or chew for a long time, and may choke on solid food.

    As the child grows up, the diagnosis is made on the basis of the following speech symptoms: persistent pronunciation defects, insufficiency of voluntary articulation, vocal reactions, incorrect placement of the tongue in the oral cavity, voice formation disorders, speech breathing and delayed speech development.

    The main signs used for differential diagnosis include:

    The presence of weak articulation (insufficient bending of the tip of the tongue upward, tremor of the tongue, etc.);

    Presence of prosodic disorders;

    The presence of synkinesis (for example, movements of the fingers that occur when moving the tongue);

    Slowness of the tempo of articulations;

    Difficulty maintaining articulation;

    Difficulty in switching articulations;

    Persistence of disturbances in the pronunciation of sounds and difficulty in automating the delivered sounds.

    Functional tests also help to establish a correct diagnosis. For example, a speech therapist asks a child to open his mouth and stick out his tongue, which should be held motionless in the middle. At the same time, the child is shown an object moving laterally, which he needs to follow. The presence of dysarthria during this test is indicated by the movement of the tongue in the direction in which the eyes move.

    When examining a child for the presence of dysarthria, special attention must be paid to the state of articulation at rest, during facial movements and general movements, mainly articulatory. It is necessary to pay attention to the volume of movements, their pace and smoothness of switching, proportionality and accuracy, the presence of oral synkinesis, etc.

    Dysarthria treatment

    The main focus of treatment for dysarthria is the development of normal speech in the child, which will be understandable to others and will not interfere with communication and further learning of basic writing and reading skills.

    Correction and therapy for dysarthria must be comprehensive. In addition to constant speech therapy work, medication treatment prescribed by a neurologist and exercise therapy are also required. Therapeutic work should be aimed at treating three main syndromes: articulation and speech breathing disorders, voice disorders.

    Drug therapy for dysarthria involves the prescription of nootropics (for example, Glycine, Encephabol). Their positive effect is based on the fact that they specifically affect the higher functions of the brain, stimulate mental activity, improve learning processes, intellectual activity and memory of children.

    Physiotherapy exercises consist of regular special gymnastics, the effect of which is aimed at strengthening the facial muscles.

    Massage has proven itself well for dysarthria, which must be done regularly and daily. In principle, massage is the first step in treating dysarthria. It consists of stroking and lightly pinching the muscles of the cheeks, lips and lower jaw, bringing the lips together with the fingers in a horizontal and vertical direction, massaging the soft palate with the pads of the index and middle fingers for no more than two minutes, and movements should be forward and backward. Massage for dysarthria is needed to normalize the tone of the muscles that take part in articulation, reduce the manifestation of paresis and hyperkinesis, activate poorly working muscles, and stimulate the formation of areas of the brain responsible for speech. The first massage should take no more than two minutes, then gradually increase the massage time until it reaches 15 minutes.

    Also, to treat dysarthria, it is necessary to train the child’s respiratory system. For this purpose, exercises developed by A. Strelnikova are often used. They involve sharp inhalations when bending over and exhalations when straightening up.

    A good effect is observed with self-study. They consist in the fact that the child stands in front of a mirror and trains to reproduce the same movements of the tongue and lips that he saw when talking with others. Gymnastics techniques to improve speech: open and close your mouth, stretch your lips like a “proboscis,” hold your mouth in an open position, then in a half-open position. You need to ask the child to hold a gauze bandage between his teeth and try to pull the bandage out of his mouth. You can also use a lollipop on a shelf that the child must hold in his mouth and the adult must take it out. The smaller the lollipop, the more difficult it will be for the child to hold it.

    The work of a speech therapist for dysarthria consists of automating and staging the pronunciation of sounds. You need to start with simple sounds, gradually moving on to sounds that are difficult to articulate.

    Also important in the treatment and correction of dysarthria is the development of fine and gross motor skills of the hands, which are closely related to speech functions. For this purpose, finger gymnastics, assembling various puzzles and construction sets, sorting small objects and sorting them out are usually used.

    The outcome of dysarthria is always ambiguous due to the fact that the disease is caused by irreversible disturbances in the functioning of the central nervous system and brain.

    Correction of dysarthria

    Corrective work to overcome dysarthria must be carried out regularly along with drug treatment and rehabilitation therapy (for example, treatment and preventive exercises, therapeutic baths, hirudotherapy, acupuncture, etc.), which is prescribed by a neurologist. Non-traditional correction methods have proven themselves well, such as dolphin therapy, isotherapy, touch therapy, sand therapy, etc.

    Correctional classes conducted by a speech therapist imply: development of motor skills of the speech apparatus and fine motor skills, voice, formation of speech and physiological breathing, correction of incorrect sound pronunciation and consolidation of assigned sounds, work on the formation of speech communication and expressiveness of speech.

    The main stages of correctional work are identified. The first stage of the lesson is a massage, with the help of which the muscle tone of the speech apparatus develops. The next step is to conduct an exercise to form correct articulation, with the goal of subsequently correctly pronouncing sounds by the child, to produce sounds. Then work is carried out on automation of sound pronunciation. The last stage is learning the correct pronunciation of words using already supplied sounds.

    Equally important for a positive outcome of dysarthria is the psychological support of the child from loved ones. It is very important for parents to learn to praise their children for any of their achievements, even the smallest ones. The child must be given a positive incentive for independent study and confidence that he can do anything. If a child has no achievements at all, then you should choose a few things that he does best and praise him for them. A child should feel that he is always loved, regardless of his victories or losses, with all his shortcomings.

    People without medical education can hardly imagine what the hypoglossal nerve is. But in some cases this information can be very important. There are a number of problems that impair a person's quality of life associated with the tongue and hypoglossal nerve. Let's take a closer look at them.

    Just something complicated

    The hypoglossal nerve innervates, that is, it connects the nerve endings of the tongue with the central nerve. It provides motor (efferent) innervation, allowing the central nervous system to control the activity of the tongue and the orbicularis oris muscle. The nerve is paired; it emerges from the anterolateral sulcus, and its core is located along the medulla oblongata.

    The mylohyoid nerve sends impulses and provides activity to the superior, inferior, longitudinal, transverse and vertical muscles. It is responsible for the movement of the genioglossus, hyoglossus and styloid muscles.

    How to understand a doctor. Meaning of terms

    Since information about the hypoglossal nerve is a little difficult to understand, patients do not always understand what the specialist is talking about. To understand the diagnosis, you need to know some terms:

    1. Hemiglossoplegia. This term refers to paralysis of half the tongue.
    2. Glossoplegia is a state of complete paralysis of the tongue.
    3. "Dysarthria." A diagnosis indicating a violation of articulate speech. Slurring is accompanied by a sensation of a foreign substance in the mouth.
    4. “Anarthria” is a diagnosis that specifies that articulate speech is impossible.

    These terms appear quite frequently in medical histories related to the hypoglossal nerve. It is better to remember their meaning.

    What does the patient complain about?

    When visiting a doctor, patients mainly complain of tongue weakness. They have difficulty speaking and sometimes even swallowing. Gradually the problem grows, and the tongue moves worse and worse. The patient may feel as if he has a “mouthful of porridge” that makes his speech difficult to understand. In difficult cases, speech disappears completely.

    Medical examination

    If a specialist suspects that the hypoglossal nerve is affected, he will determine the symptoms by examining the tongue in the oral cavity. First of all, the doctor asks you to stick out your tongue. Don't be surprised, this simple action can indicate the underlying problem. The doctor will be able to visually determine the extent of the disease. If the hypoglossal nerve does not function well, the tongue deviates to the side. This is due to muscle hypotonia on one side. The entire surface of the organ looks wrinkled and becomes uneven. But here it must be taken into account that many patients purposefully tilt their tongue towards the doctor so that he can better examine it. If there is any doubt as to whether the tongue is voluntarily or involuntarily rejected, the patient is asked to touch the upper lip with the tip. If there is no pathology, then the tip will be located in the middle, if the nerve is affected, it will move to the side.

    In addition to deviation, the doctor should pay attention to atrophy and fibrillary twitching.

    Bilateral damage to the hypoglossal nerve is observed in approximately 20% of cases. This disease is less treatable and can lead to complete loss of speech.

    Diagnosis options. Neuropathy

    Essentially, neuropathy is a nerve damage that is non-inflammatory in nature. In the case of the hypoglossal nerve, this diagnosis is divided into central and peripheral neuropathy.

    The central one affects the corticonuclear pathways of the nerve. The problem affects the cortex and nucleus of the twelfth pair of cranial nerves. This type of neuropathy is usually associated with facial nerve problems. When protruding, the tongue deviates in the direction opposite to the lesion, since the nucleus of the hypoglossal nerve has connections with the opposite hemisphere. Atrophy and fibrillary twitching are not observed.

    The process may have several stages. If the hypoglossal nerve is affected only in the area of ​​the internal section, then only the functions of the lingual muscles are affected.

    If the lesion begins below the exit of the hypoglossal nerve canal, then the problem affects the nerve fibers connected to the cervical roots. This leads to disruption of the functioning of the muscles that hold the larynx. When swallowing, there will be a shift to the healthy side.

    Peripheral neuropathy

    Signs: immobility of the epiglottis, larynx and soft palate, change in voice, loss of intelligible speech, difficulty swallowing (liquid food can flow into the nose), difficulty breathing. The vocal cords are in a “cadaverous position”, the tongue twitches fibrillarly. If the facial and trigeminal nerves are additionally affected, the masticatory muscles atrophy and the lower jaw sag.

    Very similar to bulbar, but it is a lesion of the corticonuclear connections on both sides. A larger number of cranial nerves are affected, including the hypoglossal nerve. Symptoms include drooling, reflex movements of the eyeballs, bouts of crying or laughter, dementia and decreased intelligence.

    Diagnostic methods and treatment

    The doctor collects anamnesis, performs a visual examination, and prescribes a CT or MRI of the brain to confirm the diagnosis. This allows us to find out the cause of compression of the hypoglossal nerve.

    Any treatment is prescribed after confirmation of the diagnosis. The main goal is a positive effect on the underlying disease. Self-medication is unacceptable!