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Wilson disease presents as a rare genetic disorder that leads to an accumulation of copper within various organs. This worsening condition can impact the liver, brain, eyes, and other systems. Symptoms vary widely and may include liver damage, neurological problems, and eye issues. Early detection and treatment are crucial in preventing the progres
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Wilson disease is a rare genetic disorder characterized by the organism's inability to properly remove excess copper. Normally, the liver plays a crucial role in regulating 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