WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease affects the rare genetic disorder that leads to the build-up of copper within multiple organs. This deteriorating condition can damage the liver, brain, eyes, and other systems. Symptoms differ widely often manifest liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in mitigating

Wilson disease presents as 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 controls copper transport within the body. Symptoms of Wilson disease vary widely and may