Wilson disease affects the rare genetic disorder that results in the build-up of copper within certain organs. This progressive condition often affect the liver, brain, eyes, and other tissues. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early diagnosis and treatment play a vital role in slowing down the advancement o… Read More

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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 passed down mutations in a gene called ATP7B, which regulates copper transport within the body. Symptoms of Wilson disease can be diverse a… Read More