hrp0094p1-79 | Fetal Endocrinology and Multisystem Disorders A | ESPE2021
Kilci Fatih
, Hurmuzlu Kozler Selen
, Jones Jeremy
, Ceylaner Serdar
, Mine Cizmecioğlu Jones Filiz
,
Introduction: Co-existence of congenital hypopituitarism and congenital hyperinsulinemia is extremely rare. We present a case of congenital hypopituitarism and hyperinsulinemic hypoglycemia with a novel FOXA2 mutation.Case: A 22-month-old girl was referred to pediatric endocrinology due to short stature. She was the first child of healthy, non-consanguineous parents with no relevant family history. Delivery was by cesarean secti...