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Wilson disease is a rare genetic illness that leads to excessive storage of copper throughout certain organs. This worsening condition can affect the liver, brain, eyes, and other systems. Symptoms differ widely often manifest liver damage, neurological problems, and eye issues. Early diagnosis and treatment are essential in slowing down the advanc
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Wilson disease is a rare genetic disorder characterized by the body's inability to properly eliminate excess copper. Normally, the liver plays a crucial role in managing copper levels, transporting 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