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Wilson disease is a rare genetic illness that leads to an accumulation of copper within certain organs. This progressive condition can damage the liver, brain, eyes, and other systems. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early identification and treatment are essential in preventing the progression of this serious dis
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Wilson disease is a rare genetic disorder characterized by the organism's inability to properly discharge excess copper. Normally, the liver plays a crucial role in managing 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