UNDERSTANDING WILSON DISEASE

Wilson disease is a rare genetic illness that leads to the build-up of copper within various organs. This deteriorating condition may damage the liver, brain, eyes, and other systems. Symptoms range widely can present as nausea, vomiting, and tremors. Early detection and treatment are essential in preventing the advancement of this serious disease.

Wilson disease presents as 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