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Wilson disease is a rare genetic disorder that leads to an accumulation of copper within certain organs. This worsening condition can affect the liver, brain, eyes, and other tissues. Symptoms vary widely and may include fatigue, jaundice, and abdominal pain. Early identification and treatment are crucial in mitigating the advancement of this debil

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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