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Wilson disease is a rare genetic condition that causes excessive storage of copper in various organs. This progressive condition can impact the liver, brain, eyes, and other systems. Symptoms vary widely and may include liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in slowing down the advanceme
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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 manifest gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and