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Wilson disease is a rare genetic illness that leads to excessive storage of copper within multiple organs. This worsening condition often impact the liver, brain, eyes, and other organs. Symptoms vary widely can present as nausea, vomiting, and tremors. Early detection and treatment are essential in slowing down the advancement of this debilitating
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Wilson disease is a rare genetic disorder characterized by the system'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 dis