Wilson's Disease: A Genetic Disorder of Copper Metabolism

Wilson disease, a inherited condition affecting copper processing, presents a unique set of manifestations. This uncommon condition causes the accumulation of copper in various parts of the body, primarily the liver, brain, and cornea. Individuals with Wilson disease may experience a varied range of symptoms, including cirrhotic failure, brain impa

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Wilson Disease: A Genetic Disorder of Copper Metabolism

Wilson disease, a hereditary disorder affecting copper metabolism, presents a complex set of signs. website This rare condition causes the build-up of copper in various tissues of the body, primarily the liver, brain, and cornea. Individuals with Wilson disease may experience a wide range of symptoms, including cirrhotic damage, cognitive impairmen

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Wilson Disease: A Genetic Disorder of Copper Metabolism

Wilson syndrome, a genetic condition affecting copper metabolism, presents a unique set of manifestations. This uncommon condition causes the accumulation of copper in various tissues of the body, primarily the liver, brain, and cornea. Patients with Wilson disease may present a diverse range of symptoms, including hepatic failure, neurological imp

read more