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Wilson disease affects the rare genetic disorder that leads to an accumulation of copper throughout various organs. This worsening condition may damage the liver, brain, eyes, and other systems. Symptoms range widely can present as fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in mitigating the progression o

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Wilson disease is a rare genetic disorder characterized by the body'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 disru