WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease presents as a rare genetic illness that results in an accumulation of copper in multiple organs. This progressive condition often impact the liver, brain, eyes, and other organs. Symptoms range widely often manifest nausea, vomiting, and tremors. Early identification and treatment are essential in slowing down the progression of this

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 regulates copper transport within the body. Symptoms of Wilson disease often app