WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease is a rare genetic disorder that leads to excessive storage of copper throughout various organs. This worsening condition can impact the liver, brain, eyes, and other systems. Symptoms range widely and may include fatigue, jaundice, and abdominal pain. Early diagnosis and treatment play a vital role in preventing the development of th

Wilson disease affects 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 ofte