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Wilson disease presents as a rare genetic illness that causes excessive storage of copper in certain organs. This deteriorating condition often impact the liver, blog culinaire brain, eyes, and other systems. Symptoms vary widely and may include nausea, vomiting, and tremors. Early diagnosis and treatment are essential in mitigating the development
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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