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Wilson disease presents as a rare genetic illness that causes excessive storage of copper within various organs. This worsening condition may affect the liver, brain, eyes, and other organs. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early identification and treatment are crucial in slowing down the advancement 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 appear gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and g