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Wilsons disease is a genetic disorder in which 1 in 40,000 individuals are affected. It is caused by a recessive gene in which copper metabolism is disordered, so it builds up in the body. This excess of copper can damage the eyes, brain, and liver. A Kayser-Fleisher ring, rust brown ring around the cornea of the eye, is the most characteristic symptom of this disease. Complications usually occur in later years and include: tremors, slurred speech, cirrhosis, clumsiness, and psychological changes. Lifelong treatment is needed for this disease. These are treatments such as Zinc (blocks copper absorption), Penicillamine, Tetrathiomolybdate, and a diet low in copper.

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5mo ago

Wilson's disease is a rare genetic disorder that causes copper to accumulate in the body, leading to damage in the liver, brain, and other organs. Symptoms can include jaundice, tremors, and neurological problems. Treatment involves medications to help remove excess copper and dietary changes to limit copper intake.

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Q: What are facts about wilsons disease?
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Is wilsons disease dominant or recessive?

Wilson's disease is recessive


How can you tell if someone has wilsons disease?

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