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Wilson disease presents as a rare genetic condition that causes excessive storage of copper throughout multiple organs. This progressive condition may affect the liver, brain, eyes, and other tissues. Symptoms range widely and may include liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in pr
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Wilson disease is a rare genetic disorder characterized by the organism's inability to properly remove excess copper. Normally, the liver plays a crucial role in managing 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 th