WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease is a rare genetic condition that leads to the build-up of copper in certain organs. This worsening condition can impact the liver, brain, eyes, and other tissues. Symptoms differ widely often manifest nausea, vomiting, and tremors. Early diagnosis and treatment play a vital role in preventing the progression of this debilitating dise

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 passed down mutations in a gene called ATP7B, which regulates copper transport within the body. Symptoms of Wilson disease vary widely and often pre