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Wilson disease is a rare genetic disorder that causes excessive storage of copper within various 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 are crucial in slowing down the advancement of this debili
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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 manifest gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and g