WILSON'S DISEASE: A COMPLETE GUIDE

Wilson disease presents as a rare genetic condition that leads to the build-up of copper within various organs. This progressive condition often impact the liver, brain, eyes, and other tissues. Symptoms vary widely can present as nausea, vomiting, and tremors. Early detection and treatment play a vital role in slowing down the progression of this

Wilson disease affects 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 caused by mutations in a gene called ATP7B, which regulates copper transport within the body. Symptoms of Wilson disease can be diverse and oft