Vacuolar dystrophy

Vacuum dystrophy is a rare hereditary disease that is characterized by the accumulation of vacuoles in blood cells and other organs. This disease is quite rare and usually affects men. The disease manifests itself in the form of various symptoms such as fatigue, pallor, high blood pressure, breathing problems and much more.

The main reason for the development of the disease is a genetic mutation. A person with vacuum dystrophy has a defect in a gene that is responsible for the production of a certain protein. This protein is essential for normal cell functioning. If it is not produced, then the cells begin to accumulate their own proteins in vacuoles.

Symptoms of vacuum degeneration may appear gradually or suddenly. For example, a person may experience pale skin, fatigue, or trouble sleeping or breathing. Later, serious illness may develop, with symptoms of pneumonia or heart failure.

Treatment for vacuum dystorophy depends on the severity of symptoms and the patient's condition. Antibiotics, anti-inflammatories, and other medications are usually recommended. In some cases, a bone marrow transplant may be necessary. However, treatment for vacuum dyssterophy usually has a temporary effect, and most patients die several years after the first symptoms appear.