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Wilson disease presents as a rare genetic condition that leads to the build-up of copper in various organs. This worsening condition may affect the liver, brain, eyes, and other organs. Symptoms differ widely often manifest liver damage, neurological problems, and eye issues. Early detection and treatment play a vital role in preventing the develop
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Wilson disease is a rare genetic disorder characterized by the organism'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 disru