Print ISSN: 2394-2746
Online ISSN: 2394-2754
CODEN : IJOGCS
Indian Journal of Obstetrics and Gynecology Research (IJOGR) open access, peer-reviewed quarterly journal publishing since 2014 and is published under auspices of the Innovative Education and Scientific Research Foundation (IESRF), aim to uplift researchers, scholars, academicians, and professionals in all academic and scientific disciplines. IESRF is dedicated to the transfer of technology and research by publishing scientific journals, research content, providing professional’s membership, and conducting conferences, seminars, and award more...Case Report
Author Details :
Volume : 11, Issue : 2, Year : 2024
Article Page : 301-303
https://doi.org/10.18231/j.ijogr.2024.057
Abstract
Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare congenital disorder characterised by absence of uterus and vagina. Ovaries and fallopian tubes are normal and functional. Its incidence is 1 in 4500-5000 female. Patients present with primary amenorrhea with normal external genitalia and development of secondary sexual characteristics, and 46XX karyotype. It is usually diagnosed by MRI, CT or transabdominal USG, with MRI being the gold standard.
Keywords: Mullerian agenesis, MRKH syndrome, Primary amenorrhea, Dyspareunia, Davydov, Vaginoplasty.
How to cite : Chandekar A S, Shah S R, George M, Vaghela R, A case of Mayer-Rokitansky-Kuster- Hauser syndrome type I. Indian J Obstet Gynecol Res 2024;11(2):301-303
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