WILSON'S DISEASE: A COMPLETE GUIDE

Wilson disease is a rare genetic condition that leads to the build-up of copper within various organs. This deteriorating condition often affect the liver, brain, eyes, and other organs. Symptoms range widely and may include nausea, vomiting, and tremors. Early detection and treatment play a vital role in slowing down the development of this debili

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 inherited mutations in a gene called ATP7B, which regulates copper transport within the body. Symptoms of Wilson disease vary widely and might