WILSON DISEASE: A COMPREHENSIVE OVERVIEW

Wilson disease is a rare genetic condition that causes excessive storage of copper throughout certain organs. This worsening condition may impact the liver, brain, eyes, and other systems. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early detection and treatment play a vital role in mitigating the adva

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