Wilson disease is a rare genetic condition that causes an accumulation of copper within various organs. This deteriorating condition can damage the liver, brain, eyes, and other organs. Symptoms differ widely often manifest liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in slowing down the progr

Wilson disease affects a rare genetic disorder that causes excessive copper to accumulate in the liver, brain, and other organs. This buildup can serious health problems if left untreated. The condition is caused by mutations in a gene called ATP7B, which is responsible for copper transport within the body. Symptoms of Wilson disease vary widely a