WILSON'S DISEASE: A COMPLETE GUIDE

Wilson disease is a rare genetic illness that leads to excessive storage of copper throughout various organs. This deteriorating condition often affect the liver, brain, eyes, and other organs. Symptoms vary widely and may include fatigue, jaundice, and abdominal pain. Early identification and treatment play a vital role in slowing down the develop

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 passed down mutations in a gene called ATP7B, which regulates copper transport within the body. Symptoms of Wilson disease often appear gradual