WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease is a rare genetic disorder that causes the build-up of copper throughout various organs. This deteriorating condition can damage the liver, brain, eyes, and other systems. Symptoms range widely often manifest liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in preventing the develop

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