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Mayer-Rokitansky-Küster-Hauser Syndrome: About Two Cases | OMICS International| Abstract
ISSN:2167-7964

OMICS Journal of Radiology
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  • Case Report   
  • OMICS J Radiol 2023, Vol 12(9): 485
  • DOI: 10.4172/2167-7964.1000485

Mayer-Rokitansky-K�ster-Hauser Syndrome: About Two Cases

Soufiane Rostoum*, Eric Michel Kessi, Meryem Zhim, El Amrani Soukaina, Amine Naggar, Siham El Haddad, Nazik Allali and Latifa Chat
Pediatric Radiology department, Children's Hospital, University Hospital of Ibn Sina Rabat, Morocco
*Corresponding Author : Soufiane Rostoum, Pediatric Radiology department, Children's Hospital, University Hospital of Ibn Sina Rabat, Morocco, Email: rostoum.soufiane@gmail.com

Received Date: Aug 25, 2023 / Published Date: Sep 25, 2023

Abstract

Rokitansky syndrome (MRKH) is a rare congenital disorder characterized by the absence of a uterus and at least the upper 2/3 of the vagina in women with normal development of secondary sexual characteristics. C’est une cause rare d’aménorrhée primaire qui reste le principal signe clinique. It is a rare cause of primary amenorrhea, which remains the main clinical sign. Diagnosis is based primarily on magnetic resonance imaging (MRI). We present two cases of MRKH who both consulted for primary amenorrhea, with secondary sexual characteristics present and well developed.

Citation: Rostoum S, Kessi EM, Zhim M, Soukaina EA, Naggar A, et al. (2023) Mayer-Rokitansky-Küster-Hauser Syndrome: About Two Cases. OMICS J Radiol 12: 485. Doi: 10.4172/2167-7964.1000485

Copyright: © 2023 Rostoum S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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