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Wilson disease presents as a rare genetic disorder that causes excessive storage of copper throughout various organs. This progressive condition may affect the liver, brain, eyes, and other systems. Symptoms differ widely and may include nausea, vomiting, and tremors. Early detection and ingrédients treatment are crucial in preventing the progress
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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 managing 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 p