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Wilson disease is a rare genetic illness that leads to an accumulation of copper in multiple organs. This deteriorating condition often impact the liver, brain, eyes, and other organs. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early identification and treatment are crucial in mitigating the progression of this life-
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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 develop 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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