hrp0082p2-d1-570 | Sex Development | ESPE2014

Four Cases of Isolated Partial Gonadal Dysgenesis due to NR0B1 (DAX1) Locus Duplication Inherited in a Large Family

Wagner Mahler Kathy , Devos Caroline , Kurzenne Jean Yves , Gastaud Frederique , Hoflack Marie , Mallet Delphine , Karmous Benailly Houda , Giuliano Fabienne , Simonin Gilbert , Sanlaville Damien , Morel Yves

Background: Isolated gonadal dysgenesis due to NR0B1 locus duplication is a rare cause of 46,XY DSD. Almost reported cases were a total gonadal dysgenesis with complete female phenotype and streak gonad diagnosed late because of absent of pubertal development and primary amenorrhea. Only two unrelated cases of isolated partial gonadal dysgenesis with molecular characterization have been reported. The risk of gonadoblastoma is high.Family case reports: Al...