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Wilson disease is a rare genetic illness that results in excessive storage of copper within various organs. This progressive condition can impact the liver, brain, eyes, and other systems. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early detection and treatment play a vital role in mitigating the progression of this life-thr
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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 serious 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 g
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