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Wilson disease is a rare genetic illness that causes an accumulation of copper within certain organs. This worsening condition can affect the liver, brain, eyes, and other tissues. Symptoms range widely can present as fatigue, jaundice, and abdominal pain. Early diagnosis and treatment are crucial in mitigating the advancement of this life-threaten
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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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