UNDERSTANDING WILSON DISEASE

Wilson disease presents as a rare genetic disorder that leads to excessive storage of copper within certain organs. This deteriorating condition often affect the liver, brain, eyes, and other tissues. Symptoms differ widely can present as fatigue, jaundice, and abdominal pain. Early diagnosis and treatment play a vital role in preventing the advanc

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 is responsible for copper transport within the body. Symptoms of Wilson disease