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Wilson disease presents as a rare genetic disorder that leads to the build-up of copper in certain organs. This progressive condition may impact the liver, brain, eyes, and other systems. Symptoms range widely often manifest fatigue, jaundice, and abdominal pain. Early identification and treatment are crucial in mitigating the progression of this l
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Wilson's disease is a rare genetic disorder that causes a buildup of copper in the body. This can lead to serious damage to the liver, brain, and other organs. Symptoms often manifest gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and
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