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Wilson disease presents as a rare genetic illness that causes excessive storage of copper within certain organs. This progressive condition often damage the liver, brain, eyes, and other systems. Symptoms range widely and may include nausea, vomiting, and tremors. Early diagnosis and treatment are crucial in slowing down the development of this lif
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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 appear gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and gen
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