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Wilson disease presents as a rare genetic disorder that results in excessive storage of copper throughout certain organs. This progressive condition can damage the liver, brain, eyes, and other tissues. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early identification and treatment are essential in mitigating the deve
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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