Vol. 8 (04) pp. 1134-1137 DOI: 10.21474/IJAR01/10888

CRYPTORCHIDISM AND 46 XY MALE GONADAL DYSGENESIS LAPAROSCOPIC DIAGNOSISABOUT A CASE

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  • Peadiatric Urology Department, Rabat Childrens Hospital, Ibn Sina UHC / Mohammed V University, Faculty of Medicine and Pharmacy, Rabat, Morocco.
  • Pediatric Plastic Unity, Rabat Childrens Hospital, Ibn Sina UHC / Mohammed V university, Faculty of Medicine and Pharmacy, Rabat, Morocco.
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Abstract

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.

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How to Cite This Article

Freddy Niyongere, Yassine Zouirech, Abir Manni, Zakarya Alami Hassani, Driss Hanine, Naoufal Fejjal, Mohamed Rami, Rachid Belkacem and Mohamed Amine Bouhafs (2020); CRYPTORCHIDISM AND 46 XY MALE GONADAL DYSGENESIS LAPAROSCOPIC DIAGNOSISABOUT A CASE, Int. J. of Adv. Res., 8 (04), 1134-1137, ISSN 2320-5407. DOI: https://doi.org/10.21474/IJAR01/10888

Corresponding Author

Niyongre Freddy
Peadiatric surgery
Creative Commons Attribution 4.0 This work is licensed under a Creative Commons Attribution 4.0 International License.