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Wilson disease affects the rare genetic disorder that leads to excessive storage of copper in certain organs. This progressive condition often damage the liver, brain, eyes, and other systems. Symptoms range widely can present as liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in preventing

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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 regulating copper levels, moving 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 this