Wilson disease affects the rare genetic illness that leads to excessive storage of copper within various organs. This progressive condition can affect the liver, brain, eyes, and other systems. Symptoms range widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment are crucial in preventing the progression of … Read More

Wilson disease presents as a rare genetic illness that results in the build-up of copper within various organs. This progressive condition often damage the liver, brain, eyes, and other systems. Symptoms differ widely can present as nausea, vomiting, and tremors. Early diagnosis and treatment are crucial in mitigating the development of this life-t… Read More

Wilson disease is 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 regulates copper transport within the body. Symptoms of Wilson disease vary widely and might encom… Read More