Wilson disease presents as a rare genetic illness that results in excessive storage of copper throughout multiple organs. This deteriorating condition often damage the liver, brain, eyes, and other systems. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early diagnosis and treatment are crucial in mitigating the advance

Wilson disease is a rare genetic disorder that causes excessive copper to accumulate in the liver, brain, and other organs. This buildup may serious health problems if left untreated. The condition is passed down mutations in a gene called ATP7B, which controls copper transport within the body. Symptoms of Wilson disease often appear gradually and