Brill-Simmers Disease

Brill-Simmer disease, also known as Brill-Simpson syndrome, is a rare inherited disorder that affects the skin, eyes, and internal organs.

This disease was first described by the American physician John Bril and the American pathologist Charles Simmers in the 19th century. In 1956, the genetic mutation that causes this disease was isolated.

Brill-Simmen disease manifests itself in the form of various symptoms, such as:

– Thickening of the skin on the face, arms and legs, as well as on other parts of the body.
– Change in skin color, which may be darker or lighter than usual.
– Formation of scars on the skin and subcutaneous tissue.
– Loss of vision due to damage to the retina.
– Disturbances in the functioning of the heart, lungs and other organs.

Treatment for this disease involves surgical removal of the affected tissue, as well as the use of medications to maintain health. However, since Brillat-Simmen disease is hereditary, treatment may not be effective.

Although Brillat-Simme disease is a rare disease, it can cause serious health problems and requires prompt treatment. If you suspect Brill-Simmen disease, you should see a doctor for diagnosis and treatment.

Brill-Simomers (BSB) is a rare disease that belongs to a group of hereditary forms of cerebral palsy. To date, it has been proven that 43 genetic defects lead to this disease. As a result of the defect, the child experiences a violation of motor functions of the hemipa type