hrp0082p3-d1-704 | Diabetes | ESPE2014
Tolga Ozgen Ilker
, Kucukkoc Mehmet
, Houghton Jayne
, Gokce Selim
, Cesur Yasar
Background: Neonatal diabetes is a rare disease having usually a genetic origin. Defects in KCNJ11, ABCC8, INS, GCK, and PDX1 genes are more frequent and may lead non-transient, non-syndromic neonatal diabetes, whereas defects in PTF1A, FOXP3, EIF2AK3, GLIS3, RFX6, and NEUROD1 genes are very rare and may lead neonatal diabetes as a part of a syndrome.Objective and hypotheses: We present a patient with GLIS3 ge...