Wilson disease presents as a rare genetic condition that results in the build-up of copper throughout certain organs. This progressive condition may damage the liver, brain, eyes, and other systems. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment are essential in slowing down the advancement… Read More

Wilson disease affects the rare genetic illness that leads to excessive storage of copper throughout various organs. This progressive condition often impact the liver, brain, eyes, and other tissues. Symptoms differ widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment play a vital role in mitigating the pr… Read More

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 passed down mutations in a gene called ATP7B, which is responsible for copper transport within the body. Symptoms of Wilson disease vary wi… Read More