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Wilson disease is a rare genetic illness that results in an accumulation of copper within certain organs. This deteriorating condition often impact the liver, brain, eyes, and other tissues. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early identification and treatment are essential in mitigating the development of this life-
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Wilson disease is a rare genetic disorder characterized by the body's inability to properly eliminate 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 disru