Wilson disease affects the rare genetic disorder that results in an accumulation of copper in multiple organs. This deteriorating condition may impact the liver, brain, eyes, and other tissues. Symptoms vary widely and may include fatigue, jaundice, and abdominal pain. Early detection and treatment are essential in preventing the progression of thi

Wilson disease affects 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 caused by mutations in a gene called ATP7B, which controls copper transport within the body. Symptoms of Wilson disease can be diverse and may