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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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Thus, we would not expect GLP-1 RA treatment status itself to be associated with differences in specialist visit frequency or other factors that would increase the likelihood of receiving a legal blindness code

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