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Wilson disease presents as a rare genetic disorder that results in the build-up of copper within various organs. This worsening condition often affect the liver, brain, eyes, and other organs. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment are crucial in preventing the progression of th
Wilson disease presents as a rare genetic disorder that leads to excessive storage of copper within multiple organs. This progressive condition often impact the liver, brain, eyes, and other organs. Symptoms differ widely often manifest liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in preventin
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 is responsible for copper transport within the body. Symptoms of Wilson disease can be di