hrp0084p3-719 | Diabetes | ESPE2015

Fanconi-Bickel Syndrome due to a Novel SLC2A2 Mutation Presenting with Transient Neonatal Diabetes

Elmaogullari Selin , Demirel Fatma , Tepe Derya , Dincel Nida , Tayfun Meltem , Ucakturk Seyit Ahmet , Gurbuz Fatih , Jayne Houghton

Background: Fanconi-Bickel syndrome (FBS) is a glycogen storage disease caused by the homozygous mutations of SLC2A2 gene which codes GLUT2 protein. It is characterized by growth retardation, hepatomegaly and hypophosphataemic rickets. While most of the cases with FBS have fasting hypoglycaemia and postprandial hyperglycaemia, only few cases had been shown to have neonatal diabetes (ND).Case presentation: A 14 days old girl was admitted to hospital with ...