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Wilson disease presents as a rare genetic condition that causes the build-up of copper in multiple organs. This progressive condition may impact the liver, brain, eyes, and other tissues. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in preventing the progression of this
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Wilson's disease is a rare genetic disorder that causes a buildup of copper in the body. This can lead to severe damage to the liver, brain, and other organs. Symptoms often develop gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and ge