UNDERSTANDING WILSON DISEASE

Wilson disease presents as a rare genetic illness that leads to an accumulation of copper in certain organs. This worsening condition often affect the liver, brain, eyes, and other tissues. Symptoms differ widely can present as nausea, vomiting, and tremors. Early identification and treatment play a vital role in preventing the advancement of this

Wilson disease presents as a rare genetic disorder that causes excessive copper to accumulate in the liver, brain, and other organs. This buildup can 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 oft