ea0073pep8.4 | Presented ePosters 8: Pituitary and Neuroendocrinology | ECE2021
Sertedaki Amalia
, Tatsi Elizabeth
, Vassilakis Ioannis Anargyros
, Nikaina Eirini
, Fylaktou Eirini
, Iacovidou Nikoletta
, Siahanidou Soultana
, Kanaka-Gantenbein Christina
Background CPHD is characterized by GH and at least one other pituitary hormone deficiency. Mutations in genes expressed in the developing head, hypothalamus, and/or pituitary cause CPHD. To date around 30 genes have been identified to be related to CPHD, however 85% of the cases remain with unknown molecular aetiology.Patient and methodsA newborn boy (46, XY) delivered by CS due to IUGR with a birthweight of...