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Wilson Disease: A Comprehensive Overview
Wilson disease is a rare genetic disorder that results in an accumulation of copper throughout various organs. This worsening condition often impact the liver, brain, eyes, and other tissues. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early diagnosis and treatment are crucial in mitigating the development of this deb
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Grasping Wilson's Disease: Symptoms, Diagnosis, and FMC Treatment
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 develop gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and