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Wilson disease presents as a rare genetic condition that results in the build-up of copper within various organs. This worsening condition can impact the liver, brain, eyes, and other tissues. Symptoms range widely can present as fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in slowing down the development o
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly eliminate excess copper. Normally, the liver plays a crucial role in what is wilson disease 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