Amyotrophy

Amyotrophy is a neurological disease characterized by gradual loss of muscle mass and weakening of muscles. This pathology is associated with a disease of the nerve that excites the affected muscle.

Amyotrophy is a characteristic symptom of any chronic neuropathy. Neuropathy is a disease of the peripheral nervous system that can be caused by various causes such as infections, injuries and toxic substances. Amyotrophy may be the most obvious neurological manifestation of diabetes mellitus and meningovascular syphilis.

The combination of amyotrophy and muscle spasm can be observed in various forms of motor nerve diseases. Motor nerves are the nerves that control muscle movement and provide communication between the muscles and the brain.

Symptoms of amyotrophy may include muscle weakness, loss of muscle mass, cramps, muscle and skeletal pain, and loss of coordination. Depending on the cause of the disease, amyotrophy can progress quickly or slowly, and it can be temporary or permanent.

Various methods are used to diagnose amyotrophy, including electromyography (EMG) and muscle biopsy. Treatment for amyotrophy depends on its cause and may include physical therapy, drug therapy, surgery, and other methods.

In conclusion, amyotrophy is a serious disease that can lead to significant impairment of motor function. It is important to see a specialist at the first signs of muscle loss and muscle weakness to receive timely diagnosis and treatment.

Amyotrophy is often called by its second name - “Lerrand-Nodiac disease”. This disease first began to be studied back in the 60s of the twentieth century. During that period, some German doctors discovered a violation of the development of limbs in children, but for a long time they could not find out the exact cause.

Later attention to this

Amyotrophic lateral sclerosis (ALS)

Amyotrophic Lateral Sclerosis, also known as ALS, is a progressive neurodegenerative disease that affects nerve cells and muscles in the body. The common symptoms include muscle weakness, spasticity, atrophy, and respiratory difficulties, which can lead to death within five years of diagnosis. The disease is characterized by the loss of motor neurons in the spinal cord and brainstem, leading to progressive paralysis of both upper and lower limbs. Among other signs, patients may also experience sensory symptoms such as numbness, tingling, and burning sensations, caused by damage to the peripheral nervous system. The earliest signs of ALS are subtle and may be overlooked or misdiagnosed, including fatigue, loss of strength, and a slight loss of coordination. Once the disease progresses, it can have life-threatening consequences such as trouble breathing and swallowing, which require specialized medical care. Diagnosis

Amyotrophic sclerosis, or otherwise Amyotrophy, a neurological disease, the main part of the symptoms of which is progressive damage to the peripheral nervous system, leading to gradual muscle atrophy

Amyotrophy is a disorder of the nervous system. It can cause numbness and weakness in muscles throughout the body. The type of defect depends on the location in your nervous system where the disease develops

According to statistics, about 5-10% of people on the planet suffer from amyotrophy. Moreover, in 80-90% of cases, genetic factors are to blame for its development. 70-80% of patients die from amyotrophic sclerosis at the first stage of the disease, when the diaphragm atrophies; in total, the disease lasts an average of 4 years

There is no specific therapy for amyotrophosis. Doctors can only alleviate its course, but not cure the disease. Paralympic events, trainings, social adaptation support patients