Wilson disease is a rare genetic disorder that causes excessive storage of copper in multiple organs. This progressive condition may affect the liver, brain, eyes, and other organs. Symptoms range widely and may include nausea, vomiting, and tremors. Early detection and treatment are crucial in slowing down the progression of this serious disease.

Wilson disease affects 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 inherited mutations in a gene called ATP7B, which controls copper transport within the body. Symptoms of Wilson disease often appear gra