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Wilson disease affects the rare genetic illness that leads to an accumulation of copper throughout various organs. This deteriorating condition often impact the liver, brain, eyes, and other tissues. Symptoms range widely can present as nausea, vomiting, and tremors. Early identification and treatment are essential in mitigating the development of
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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, 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