Charcot-Marie Amyotrophy

Charcot Marie Amyotrophyosis is a severe neurological disease characterized by the progressive loss of muscle tissue. With this disease, degradation of the nervous system is observed, which leads to a disorder of functional activity. Symptoms of the disease appear mainly between 20 and 50 years of age, but can also appear at an earlier age.

Charcot Marie Amytrophyosis affects many people from different countries and nationalities, as well as different social strata of the population. However, its diagnosis and treatment remains challenging. In this article we will look at some aspects of this disease.

Causes and symptoms of Charcot Marie Amatofia

Charcot-Mayotrophy refers to hereditary motor diseases. The disease is based on progressive muscular dystrophy, which is accompanied by secondary changes in various organs. Children with signs of hereditary muscular dystrophy require timely comprehensive medical and social rehabilitation. Numerous forms of myopathy and syndromic diseases lead to the formation of dwarf and disproportionate phenotypes. In this case, muscle function suffers, secondary deformations of the chest, legs, arms, spine, scoliosis, retraction of the larynx develop, self-care skills are impaired, etc. All these changes are aggravated by subsequent disability and often premature death in patients with Colley syndrome

Charcot Marie Amyotrophy is a hereditary disease that affects the peripheral nervous system. This disease is characterized by slow damage to skeletal muscles and nerves, resulting in poor coordination, difficulty walking, and progressive muscle weakness.

The cause of myopathic neurons is unknown in many cases. There are suggestions that there is a genetic predisposition for the development of Charcot-Marie-Thomas syndrome. The familial model is considered the most common form of the disease, as indicated by data from a large study of patient pedigrees conducted in Israel. It is possible, however, that the family model is a rare phenomenon; The familial nature of the disease is evidenced by isolated cases of the occurrence of familial syndrome under the influence of