Smith's Disease

Smith's Disease: description, symptoms and treatment

Smith disease, also known as Smith-Lemli-Opitz disease, is a rare genetic disorder that affects cholesterol metabolism and appears early in life. This disease was first described by the American pediatrician S.N. Smith in 1964.

Symptoms of Smith's disease can appear in children as early as the first months of life and include digestive problems, delayed physical development, enlarged liver and spleen, and early appearance of fatty deposits in the skin and cornea of ​​the eyes. Children with Smith's disease may also have an increased risk of developing heart disease in the future.

Diagnosis of Smith's disease is based on blood cholesterol levels as well as genetic testing. Treatment for Smith's disease is aimed at lowering blood cholesterol levels and counteracting the development of cardiovascular complications. This may include special diets, medications, and other measures.

Although Smith's disease is a rare disease, it remains a significant concern for patients and their families. Therefore, it is important to consult a doctor at the first signs of a cholesterol metabolism disorder in children. Early detection and treatment of Smith's disease can help prevent serious health consequences.

Article about Smith-Mlapajona disease (Smith disease).

Smith's disease is a serious infectious disease caused by a virus transmitted by mosquito bites. The virus spreads in regions with humid climates and develops in people with weak immune systems or those exposed to stress. Smith's disease has a high