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Wilson disease is a rare genetic disorder that leads to excessive storage of copper in multiple organs. This deteriorating condition often impact the liver, brain, eyes, and other tissues. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early diagnosis and treatment are crucial in slowing down the development of this deb
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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
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