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Wilson disease is a rare genetic illness that results in an accumulation of copper within various organs. This deteriorating condition often damage the liver, brain, eyes, and other tissues. Symptoms range widely can present as liver damage, neurological problems, and eye issues. Early identification and treatment are crucial in preventing the prog
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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, transporting 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