hrp0098rfc9.5 | Sex Endocrinology and Gonads | ESPE2024
Gruber Noah
, Raanani Hila
, Shani Hagit
, Segev Meirav
, Barel Ortal
, Mizrahi Sapir Rotem
, Meirow Dror
, Hourvitz Ariel
, Pinhas-Hamiel Orit
, Kedem Alon
Introduction and aims: The current guidelines for the genetic workup of primary ovarian insufficiency (POI) include performing karyotype and assessing the Fragile X carrier state (FXS). We aimed to investigate the genetic etiologies of POI and assess the need for updated guidelines for POI workup.Methods: We conducted a prospective trial that included individuals with non-iatrogenic, normal karyotype POI, referred to two...