Burgona's disease

Burgon's disease is a rare genetic disease in which a person loses control over his body and becomes a "toy in the hands of the mind." This condition is characterized by disruption of communication between the brain and muscles, resulting in loss of coordination, weakness and paralysis.

The disease manifests itself in only two percent of those affected (twice as often in men as in women). Symptoms of the disease may appear as early as the first years of life or may not appear until adolescence. As a rule, the disease begins to manifest itself between the ages of 15 and 25 years. Symptoms of Burgona may vary depending on the extent of the disease. Some people experience seizures, while others lose control of their body and move their limbs.

Historians believe that burgona was known in ancient times and many peoples fought against this disease. In ancient times, it was most often caused by the Lr gene (from the word Latin Resistance - “Latin resistance”) - the gene of the body’s immune response that resists the virus. It is found on the X chromosome and is passed from mother to daughter.

To treat Burgon's disease, medications are used to combat seizures and neurological symptoms of the disease. However, there is no cure for this disease yet. In most cases, treatment is ineffective or has an unpredictable effect.

Burgon's disease is a serious personal obstacle and a potentially fatal disease that can affect the entire life of a person and his descendants. Although the disease is still not fully understood, scientists are actively working to find ways to prevent and control the disease.