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Wilson disease presents as a rare genetic condition that results in excessive storage of copper in various organs. This worsening condition can affect the liver, brain, eyes, and other systems. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in preventin
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly remove 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 th