UNDERSTANDING WILSON DISEASE

Wilson disease is a rare genetic disorder that causes an accumulation of copper within various organs. This progressive condition may affect the liver, brain, eyes, and other tissues. Symptoms differ widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment are essential in slowing down the advancement of this

Wilson disease affects a rare genetic disorder that causes disease wilson 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 controls copper transport within the body. Symptoms of Wilson disease v