Pediatric Wilson's disease

Pediatric Wilson's disease is a rare genetic disorder where the body cannot properly eliminate copper. Normally, copper helps with various body functions, but in this condition, excess copper builds up mainly in the liver, brain, and other organs. This accumulation can damage these organs, leading to symptoms like liver problems, neurological issues, and psychiatric changes. Because it’s inherited, it often appears in childhood or adolescence. Early diagnosis and treatment, usually with medications that remove copper, are crucial to prevent serious health complications and improve quality of life.