ea0058p075 | Diabetes | BSPED2018
Elhomoudi Ayman
, Tziaferi V
, Greening James
, Sundaram Prem
Introduction: A case series of three children diagnosed with MODY at a university hospital between November 2015 and May 2018. All of them was found to have HNF1B mutation.Background: HNF1β-MODY (MODY5) is a rare form of monogenic diabetes that is often associated with a wide range of urinary tract anomalies including renal cysts. Its a dominantly inherited disease including maturity-onset diabetes of the young (MODY), pancreatic insufficiency...