Abstract
To the Editor: MUTYH (mutY homolog)–associated polyposis (MAP) is a recently discovered autosomal recessive precancerous colorectal condition caused by germline mutations in the BER (base excision repair) gene, MUTYH (MYH) (1). Its mutation spectrum and phenotype have yet to be fully elucidated. We report a case of comorbid MAP and idiopathic gastric acid hypersecretion.
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