WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease is a rare genetic condition that causes the build-up of copper in multiple organs. This deteriorating condition can impact the liver, brain, eyes, and other systems. Symptoms range widely and may include nausea, vomiting, and tremors. Early detection and treatment are essential in slowing down the advancement of this life-threatening

Wilson disease presents as 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 caused by mutations in a gene called ATP7B, which is responsible for copper transport within the body. Symptoms of Wilson disease can be di