Wilson’s disease is a disabling physical disorder that affects copper metabolism, leading to accumulation of copper in the liver, cornea and nervous system producing cirrhosis of the liver and neurological diseases. The cause is a mutation in a specific gene located on chromosome 13, a rare disease, The symptoms of the liver from jaundice, abdominal pain and other nervous system symptoms such as tremors, involuntary movements and others. The diagnosis is based on the examination of copper and syrioloplasmin in blood and urine, where it is low in the blood and high in urine, and is based on penicillin Amin.
Summary of Wilson’s disease
