UNDERSTANDING WILSON DISEASE

Wilson disease is a rare genetic illness that results in excessive storage of copper throughout certain organs. This progressive condition may damage the liver, brain, eyes, and other systems. Symptoms differ widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment are crucial in preventing the progression of this

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