UNDERSTANDING WILSON DISEASE

Wilson disease is a rare genetic illness that leads to excessive storage of copper throughout various organs. This progressive condition often damage the liver, brain, eyes, and other tissues. Symptoms range widely often manifest nausea, vomiting, and tremors. Early diagnosis and treatment play a vital role in preventing the progression of this deb

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 inherited mutations in a gene called ATP7B, which is responsible for copper transport within the body. Symptoms of Wilson disease often appear gradu