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Wilson disease is a rare genetic illness that results in the build-up of copper in certain organs. This deteriorating condition may damage the liver, brain, eyes, and other organs. Symptoms differ widely and may include liver damage, neurological problems, and eye issues. Early detection and treatment are essential in slowing down the development o
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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 severe 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 g