hrp0089p2-p192 | Fetal, Neonatal Endocrinology and Metabolism P2 | ESPE2018
, Yildiz Yilmaz
, Serap Sivri H.
, Alikasifoglu Ayfer
Introduction: Congenital disorder of glycosylation type-1a is a multi-system disease involving neurological, gastrointestinal, ophthalmologic, cardiac or endocrine systems. In addition to hypothyroidism and hypergonadotropic hypogonadism, rare occurrences of hyperinsulinemic hypoglycemia in CDG patients have been reported. In the present report, we describe a patient diagnosed with CDG type-1a accompanied by hyperinsulinemic hypoglycemia, and whose responsive to diazoxide....