the wilsons disease

Wilson's disease Wilson's disease is a hereditary disorder of chromosome 13. This disease is a hereditary disease that is likely to be present in all offspring when parents are suffering from this disease. This is an unnecessary increase in liver and brain copper. This is because there is a problem with copper transport. Wilson's disease is a rare copper transport autosomal recessive disorder that leads to copper accumulation. It is also known as liver lens degeneration as the scientific name.

Wilson's disease is an inherited disorder in which excessive copper accumulates in the body, especially the liver, brain and eyes. The signs and symptoms of Wilson's disease usually appear first between 6 and 45 years of age, but are most common in adolescence. Characteristics of this disease include a combination of liver disease and neurological and psychiatric problems. Liver disease is usually the first characteristic of Wilson's disease in sick children and young people; they may have very mild liver disease, but elderly people usually have symptoms of liver problems Is not ... Symptoms and signs of liver disease include yellowish white or white eyes (jaundice), fatigue, anorexia, swelling of the abdomen.

Wilson's disease is an autosomal recessive disorder due to a mutation in the Wilson disease protein (ATP7B) gene. For affected people, they must inherit copies of the affected genes from each parent. Diagnosis may be difficult, usually including blood tests, urinalysis, and liver biopsy. Genetic testing can be used to screen families of affected individuals. Wilson's disease is usually caused by changes in diet and medication. Changing the meal involves eating low copper diet without using copper cookware. Drugs used include chelating agents such as trientine and d-penicillamine, and zinc supplements. Complications of Wilson's disease include liver failure, liver cancer, and kidney problems. Liver transplantation may be useful for other patients with ineffective treatment or liver failure