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Wilson disease affects the rare genetic disorder that results in the build-up of copper in multiple organs. This progressive condition often impact the liver, brain, eyes, and other systems. Symptoms vary widely can present as liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in preventing the deve
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Wilson disease is a rare genetic disorder characterized by the organism's inability to properly eliminate 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