Mayer-Rokitansky-Küster-Hauser Syndrome: About Two Cases
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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