hrp0092p1-241 | Multisystem Endocrine Disorders | ESPE2019
Kurnaz Erdal
, Türkyilmaz Ayberk
, Yarali Oguzhan
, Demir Berrin
, Çayir Atilla
Background: 46,XX gonadal dysgenesis is a rare condition linked to delayed puberty, absence of spontaneous pubertal development, and primary amenorrhea related to hypergonadotropic hypogonadism (Hh). External genitalia are typically female with no ambiguity. Although ovarian development is an active process with multiple gene involvement, the genetic etiology of this condition is usually unknown. DCAF17 has recently been implicated in the development ...