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It is considered rare, with a prevalence of approximately 1 in 30,000 individuals. Geeky Medics bundles and get discounted access to all our resources in one place Aetiology Wilsons disease is an autosomal recessive disorder caused by mutations in the ATP7B gene located on chromosome 13

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Lack of Evidence Despite its popularity, its important to note that the lack of scientific evidence supporting some of the claimed benefits of IV therapy is a significant limitation

[12] Folate supplementation may affect the course and treatment of pernicious anemia if vitamin B 12 not replaced

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