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Wilson disease is a rare genetic disorder that causes the build-up of copper throughout various organs. This progressive condition may damage the liver, brain, eyes, and other systems. Symptoms differ widely often manifest liver damage, neurological problems, and eye issues. Early detection and treatment play a vital recette facile role in mitigati
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Wilson disease is a rare genetic disorder characterized by the organism'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 disru