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Wilson disease is a rare genetic illness that leads to an accumulation of copper in various organs. This deteriorating condition can affect the liver, brain, eyes, and other systems. Symptoms vary widely can present as liver damage, neurological problems, and eye issues. Early detection and treatment are essential in preventing the development of t
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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