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Wilson disease presents as a rare genetic condition that results in excessive storage of copper within various organs. This progressive condition often impact the liver, brain, eyes, and other systems. Symptoms differ widely and may include liver damage, neurological problems, and eye issues. Early detection and treatment play a vital role in slowi
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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, 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 t