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Wilson disease presents as a rare genetic condition that results in the build-up of copper in various organs. This deteriorating condition often affect the liver, wilson disease genereviews brain, eyes, and other systems. Symptoms differ widely and may include fatigue, jaundice, and abdominal pain. Early detection and treatment are crucial in preve

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Wilson disease is a rare genetic disorder characterized by the body's inability to properly discharge 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