CRYPTORCHIDISM AND 46 XY MALE GONADAL DYSGENESIS LAPAROSCOPIC DIAGNOSISABOUT A CASE

Disorders of Sex Development (DSD), formerly known as sexual ambiguity, are abnormalities leading to discrepancy between internal genital organs (IGO), external genitals (EGO) and secondary sexual characteristics. We report on a particularly complex case of 46 XY gonadal dysgenesis, monitored at the childrens hospital of Rabat, which presented a male phenotype and whose parents consult for bilateral cryptorchidism, with well-individualized male external genital organs, a male morphotype without any other clinically detectable malformation. Our goal is to contribute to the study of the rare peculiarities of sexual ambiguities, to offer a diagnostic approach to their management.