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Wilson disease is a rare genetic disorder that causes excessive storage of copper within multiple organs. This deteriorating condition often impact the liver, brain, eyes, and other tissues. Symptoms range widely and may include nausea, vomiting, and tremors. Early detection and treatment are essential in mitigating the development of this life-thr
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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 develop gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and g