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Wilson disease presents as a rare genetic condition that causes an accumulation of copper within multiple organs. This deteriorating condition may damage the liver, brain, eyes, and other tissues. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early identification and treatment play a vital role in preventing the advanc
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly eliminate excess copper. Normally, the liver plays a crucial role in processing copper levels, carrying 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