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Wilson disease affects the rare genetic condition that leads to excessive storage of copper throughout multiple organs. This progressive condition may affect the liver, brain, eyes, and other systems. Symptoms vary widely often manifest liver damage, neurological problems, and eye issues. Early identification and treatment are essential recettes fa
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly discharge excess copper. Normally, the liver plays a crucial role in regulating 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 t