hrp0092p3-202 | Pituitary, Neuroendocrinology and Puberty | ESPE2019
Kaygusuz Sare Betul
, Arslan Ateş Esra
, Kirkgöz Tarik
, Eltan Mehmet
, Abali Zehra Yavas
, Helvacioğlu Didem
, Seven Menevse Tuba
, Tosun Busra Gurpinar
, Tutar Engin
, Volkan Burcu
, Tuney Davut
, Turan Serap
, Bereket Abdullah
, Guran Tulay
Objectives: Forkhead box A2 (Foxa2) is a transcription factor that plays a key role in foregut, pancreatic and central nervous system development. Here, we describe a 7 years old boy whose phenotype is consistent with FOXA2 defect.Case: A 3 months old boy was referred for recurrent hypoglycemic events. He was born to unrelated parents at term with a birth weight of 3690 gr. At 6 hours of life he had severe hypoglycemia (...