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Wilson disease is a rare genetic disorder that leads to an accumulation of copper throughout multiple organs. This worsening condition can affect the liver, brain, eyes, and other systems. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment play a vital role in slowing down the progression o
Wilson disease is a rare genetic illness that causes the build-up of copper throughout certain organs. This progressive condition can affect the liver, brain, eyes, and other organs. Symptoms range widely often manifest nausea, vomiting, and tremors. Early identification and treatment are crucial in mitigating the development of this debilitating d
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