Banga Disease

Pain in the muscles and spine is a consequence of metabolic disorders in the muscles. The disease has several forms of manifestation: * Pain when bones and muscles are affected; * Lead myasthenia; *Analgesic effect of pain.

The main cause of the disease is called congenital metabolic defect. Inheritance occurs according to a recessive type, that is, both parents must be carriers of the disease gene. However, the “usual” manifestation of the disease occurs only against the background of an acute deficiency of cobalt, manganese, copper or vitamin C. As is known, all these substances are directly related to metabolism in muscle tissue. A deficiency of these elements leads to disruption of enzymatic processes, which provokes pain. In addition, it is known that patients with Banguet disease have a significantly increased need for vitamin C. This is partly due to the fact that it is consumed at an increased rate to maintain metabolic processes.

Banga disease is a disease caused by a violation of the normal regulation of blood circulation. This is a rare genetic disease that is characterized by changes in blood vessels in the body. The main symptoms of the disease are frequent fainting and heart disease. Banga also named the clinical picture of the disease (unfriendlyness), when the patient experiences severe headaches, insomnia, depression, indifference and indifference. He also describes the self-healing effect of the disease: vascular symptoms may disappear within minutes of the attack. For example, during painful heart attacks or hemorrhages, skin symptoms may disappear quickly, only to reappear within minutes.