WILSON'S DISEASE: A COMPLETE GUIDE

Wilson disease presents as a rare genetic condition that leads to an accumulation of copper in various organs. This worsening condition may damage the liver, brain, eyes, and other tissues. Symptoms range widely and may include nausea, vomiting, and tremors. Early identification and treatment are crucial in mitigating the advancement of this life-t

Wilson disease is 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 controls copper transport within the body. Symptoms of Wilson disease vary widely and might encomp