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Wilson disease presents as a rare genetic disorder that results in an accumulation of copper in certain organs. This progressive condition may impact the liver, brain, eyes, and other organs. Symptoms range widely and may include fatigue, jaundice, and abdominal pain. Early identification and treatment play a vital role in mitigating the developmen

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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

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