WILSON'S DISEASE: A COMPLETE GUIDE

Wilson disease is a rare genetic disorder that results in an accumulation of copper within multiple organs. This deteriorating condition may affect the liver, brain, eyes, and other tissues. Symptoms range widely and may include liver damage, neurological problems, and eye issues. Early identification and treatment are essential in preventing the d

Wilson disease affects a rare genetic disorder that causes excessive copper to accumulate in the liver, brain, and other organs. This buildup may 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 can be dive