Searchable abstracts of presentations at key conferences in endocrinology

ea0033p17 | (1) | BSPED2013

Frequency of focal and diffuse congenital hyperinsulinism with paternally inherited mutations in ABCC8 and KCNJ11

Gopal Jaya Sujatha , Mohamed Zainaba , Padidela Raja , Patel Leena , Skae Mars , Didi Mohammed , James Jackie , Caine Louise , Rigby Lindsey , Cosgrove Karen E , Dunne Mark , Ellard Sian , Banerjee Indi , Clayton Peter

Introduction: Congenital hyperinsulinism (CHI) causes severe hypoglycaemia, which can be either focal or diffuse in aetiology. Both forms are associated with paternally inherited mutations in ABCC8/KCNJ11. Lymphocytic DNA analysis alone is inadequate to diagnose focal CHI, as pancreatic maternal allelic silencing cannot be tested prior to surgery. Additional 18-fluorodopa PET–CT scanning (PET–CT) is required for definitive diagnosis; in this study, ...