Wilson disease is a rare genetic condition that results in the build-up of copper throughout multiple organs. This progressive condition may impact the liver, brain, eyes, and other systems. Symptoms range widely can present as nausea, vomiting, and tremors. Early diagnosis and treatment are crucial

Wilson disease presents as 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 inherited mutations in a gene called ATP7B, which controls copper transport within the bod