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Wilson disease is a rare genetic condition that leads to the build-up of copper in certain organs. This deteriorating condition can damage the liver, brain, eyes, and other systems. Symptoms vary widely and may include liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in mitigating the advance… Read More

Wilson disease presents as a rare genetic illness that leads to an accumulation of copper in certain organs. This worsening condition may impact the liver, brain, eyes, and other organs. Symptoms vary widely and may include liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in preventing the de… Read More

Wilson disease is 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 inherited mutations in a gene called ATP7B, which is responsible for copper transport within the body. Symptoms of Wilson disease can be diverse and… Read More