Amiotrophy: causes, treatment, prevention, exercise

The term "amyotrophy" refers to a complex of diseases, consisting in various kinds of weight loss and muscle atrophy. Violations of muscular tissue trophism are associated with lesions of cells of the brain stem, spinal nerves and spinal cord. As a result, the volume and number of muscle fibers are reduced.

Muscle fibers become thinner, and their contractility decreases. Amiotrophy is a consequence of diseases of the nervous and muscular systems. By virtue of this, neural and spinal amyotrophies are distinguished. The cause of neural amyotrophy is damage to the peripheral nerves, spinal amyotrophies cause damage to motoneutrons of the brain stem and spinal cord.

Neural amyotrophies include the neural amyotrophy of Charcot-Marie-Toot, as well as the hypertrophic neuritis of Jerin-Sott.

Clinical picture of neural amyotrophy of Charcot-Marie.

Neural amyotrophy Charcot-Marie is more common in women and is among the hereditary diseases. It manifests itself in the period from 10 to 20 years, although some symptoms of the disease can occur at an earlier age or vice versa after 30 years. The first signs of the disease may be weakness in the legs, extensor dysfunction of the thumb. In the future, the small muscles of the foot are atrophied, which causes it to sag.

Amyotrophy of Charcot-Marie is accompanied by a so-called "chicken gait."After 5-10 years, the disease covers the upper limbs, which is accompanied by the same symptoms. The hypertrophic neuropathy of Jerin-Sott is a disease that occurs rarely. The clinical picture of this disease is similar to the neural amyotrophy of Charcot-Marie. The difference is that Jerin-Sott neuropathy begins in early childhood.

Species of spinal amyotrophy

Among the spinal amyotrophies are:

1. amyotrophy of Verding-Hoffman,
2. pseudomyopathic progressive form of Kugelberg-Welander,
3. amyotrophy of Aran-Dyushenna and other rare forms.

Verdig-Hoffmann's spinal amyotrophy is divided into congenital, pediatric early and late forms of the disease. Even in the period of fetal development, there may be a later or very sluggish stirring of the fetus, which may be a sign of congenital amyotrophy. The newborn has no tendon reflexes. Not all children can sit on their own and hold the head. The disease is rapidly progressing. Eventually, there is a fatal outcome due to the weakness of the respiratory muscles.

Symptoms of early childhood form of amyotrophy appear from 6 months to 1 year. Muscular motor functions first have a normal course of development, then it stops, regression begins later, which results in bulbar paralysis. Children with this diagnosis survive only to adolescence - 15 years.

Verdnig Hoffmann Amiotrophy of the late form begins to manifest itself to 1.5 - 2 years of the child's life. The first signs are the appearance of an uncertain gait, the children are characterized by frequent falls. Further development of the disease is accompanied by a decrease in tendon reflexes, joint loosening, bulbar syndrome with dysphagia develops. By the age of 12 the disease is progressing, the children are no longer able to move independently, but they live up to about 20-30 years.

The youthful form of Kugelberg - Welander manifests itself to the age of 4 - 8 years. The initial stage of the disease is accompanied by the following symptoms: general weakness, lethargy, weakness of the lower limbs, there are difficulties with climbing the stairs. Slowly developing muscle atrophy has the property of masking subcutaneous fat deposits. Reducing muscle tone causes gait changes. The disease proceeds slowly, the activity of movement persists long enough. Over time, there are fascicular twitchings. People with this diagnosis live up to 45 years.

Treatment of amyotrophy

Treatment of amyotrophy consists in stopping the atrophy of the muscular system, and in some cases even the growth of new muscles is possible. But at once it is necessary to warn all native patients that in treatment they too should take a direct part. After all, treatment procedures are carried out not only in the hospital, but also at home. And they should be conducted daily, preferably without interruptions, otherwise all the efforts expended will be wasted.

Here is an approximate treatment regimen:

• Admission of medicines according to a specific schedule for up to twelve months
• Special diet
• Physiotherapy and massage
• Therapeutic gymnastics
• Psychological assistance to the patient
• Neuropsychological care is provided for children who are lagging behind in their psychological development due to illness.

Drug treatment is divided into three interrelated directions. The first of them is the improvement of the patient's muscles nutrition. It involves vitamins, amino acids, biostimulants. The next direction is those drugs that can stimulate the growth of muscle mass. Anabolic drugs are involved. And the third direction is the protection of muscle cells with antioxidants. Only in this way the interaction of several groups of drugs can be controlled with amyotrophy. Doses, combinations of drugs are selected individually for each patient. It depends on the age, sex and the presence of concomitant diseases.

Nutrition also plays an important role in the treatment of such patients, because the disease leads to loss of muscle mass to the sick. Therefore, with the help of food, this loss needs to be filled. This will help protein nutrition. Ideal for this are nutrient mixtures - amino acids, in which vitamins and L-carnitine are added. But sometimes some concomitant diseases prevent the absorption of proteins. Then the cause is first of all treated, because of which the protein is not taken by the patient's body.

Physiotherapy and massage are necessary to improve blood supply to weakened muscles. For example, physiotherapy remove fat and scar tissue from muscle tissue. They are formed on the site of dead muscles. Physiotherapy also helps with contractures - this is when the amplitude of joint movements decreases. When applying massage, it is necessary to take into account the specificity of the disease, because the standard methods are not suitable here. With amyotrophy, the emphasis in massage is made on weakened, inelastic parts of the muscles of the body.

When carrying out gymnastic exercises, it is necessary to take into account the characteristics of the human body. The fact that a man with the failure of one group of muscles in the work include others who take on the functions of the patient site. This can lead to a wrong course of treatment. Therefore, when carrying out gymnastic exercises, it is necessary to select those that can work out weakened muscles in isolation.

Some patients need to provide psychological help. This is especially true for adults. In the progressive form of the disease, they may have unwanted thoughts. It seems that they are of no use to anybody and are a burden. With children, psychological help is expressed in the fact that the child should be helped to develop intellectually. It's not a secret that the muscles are involved in the development of cortical functions of the brain. Through them, training signals are transmitted by writing, counting, and others. And weakened muscles can not provide the correct flow of impulses. Because of this, the child's intellectual development may lag behind the development of peers. Developing exercises can help to reduce this lag.