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Wilson disease affects the rare genetic illness that leads to an accumulation of copper throughout certain organs. This deteriorating condition may affect the liver, brain, eyes, and other organs. Symptoms differ widely often manifest nausea, vomiting, and tremors. Early diagnosis and treatment play a vital role in preventing the development of thi
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Wilson disease is a rare genetic disorder characterized by the body's inability to properly discharge excess copper. Normally, the liver plays a crucial role in processing copper levels, moving it to other parts of the body where it is needed for various functions. However, in individuals with Wilson disease, mutations in the ATP7B gene disrupt thi