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Wilson disease presents as a rare genetic disorder that leads to excessive storage of copper within certain organs. This deteriorating condition may damage the liver, brain, eyes, and other organs. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early identification and treatment are essential in slowing down the development of t
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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 critical 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