Wilson disease presents as a rare genetic condition that leads to the build-up of copper throughout various organs. This deteriorating condition often damage the liver, brain, eyes, and other organs. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early detection and treatment are crucial in slowing down the progression of this s

Wilson disease is 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 is responsible for copper transport within the body. Symptoms of Wilson disease can be diverse and