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Wilson disease is a rare genetic illness that causes an accumulation of copper throughout multiple organs. This deteriorating condition often affect the liver, brain, eyes, and other tissues. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in preventing the d

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Wilson disease is a rare genetic disorder characterized by the body'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 this