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Wilson disease affects the rare genetic disorder that results in the build-up of copper in various organs. This worsening condition can damage the liver, brain, eyes, and other organs. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in preventing the advancement of this seri
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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 processing 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 disru