hrp0094p2-14 | Adrenals and HPA Axis | ESPE2021
Gurpinar Tosun Busra
, Demirkol Yasemin Kendir
, Menevse Tuba Seven
, Kaygusuz Sare Betul
, Ozbek Mehmet Nuri
, Altincik Selda Ayca
, Mammadova Jammala
, Cayir Atilla
, Doger Esra
, Bayramoglu Elvan
, Nalbantoglu Ozlem
, Mutlu Gul Yesiltepe
, Aghayev AghaRza
, Turan Serap
, Bereket Abdullah
, Guran Tulay
,
Background: Aldosterone synthase deficiency (ASD) caused by mutations in the CYP11B2 gene is characterized by isolated mineralocorticoid deficiency. Data is scarce regarding clinical and biochemical outcomes of the disease in the follow-up.Objective: Assessment of the growth and steroid profiles of patients with ASD at the time of diagnosis and after termination of treatment.Design an...