Wilson disease is a rare genetic condition that leads to an accumulation of copper within various organs. This worsening condition may affect the liver, brain, eyes, and other tissues. Symptoms vary widely and may include fatigue, jaundice, and abdominal pain. Early detection and treatment are essential in preventing the advancement of this serious

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 body. Symptoms of Wilson disease often appear gradua