Wilson’s disease is a rare genetic disorder in which excess copper builds up in the body, leading to liver damage, neurological symptoms, and psychiatric problems. The condition occurs due to a defect in copper metabolism, impairing the liver's ability to eliminate copper. Symptoms can include fatigue, jaundice, tremors, difficulty speaking, and personality changes. Early diagnosis and treatment, typically with medications that help remove excess copper, can prevent severe complications. If left untreated, Wilson’s disease can lead to liver failure or neurological damage.
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