Wilson disease presents as a rare genetic disorder that results in the build-up of copper throughout various organs. This progressive condition can affect the liver, brain, eyes, and other systems. Symptoms range widely often manifest nausea, vomiting, and tremors. Early detection and treatment are crucial in mitigating the advancement of this life

Wilson disease is 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 is responsible for copper transport within the body. Symptoms of Wilson disease often appea