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Article

17q12 Deletion Syndrome as a Rare Cause for Diabetes Mellitus Type MODY5

18 Jul 2018

Abstract excerpt

Context: Maturity-onset diabetes of the young type 5 (MODY5) is caused by mutations of the hepatocyte nuclear factor 1 homeobox β gene (HNF1B). Although clinical characteristics and therapeutic management of MODY5 are increasingly better defined, adequate consideration of the frequent association of MODY5 with 17q12 deletion syndrome is often missing. Evidence Acquisition: We report two cases of patients with...

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Identifiers

PMID: 30032214
DOI: 10.1210/jc.2018-00955

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