Mayer-Rokitansky-Küster-Hauser syndrome type II: A rare case report [PDF]
SAGE Open Medical Case ReportsMRKH syndrome, or Mayer-Rokitansky-Küster-Hauser syndrome, a rare congenital disease, manifests as a complete or partial aplasia of the uterus and the vagina’s upper two-thirds with normal external genitalia and functioning ovaries.
Kaouthar Sfar +6 more
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Retrograde menses presented as acute stump appendicitis- Mayer-Rokitansky-Küster-Hauser syndrome [PDF]
Radiology Case ReportsMayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an exceptionally rare condition. This article highlights its unusual presentation and the role of radiological imaging in the diagnosis and outlines an approach to management.
Mohammad Mohsin Arshad, MBBS, MD +3 more
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Recurrent ovarian inguinal hernia complicated with Mayer–Rokitansky–Küster–Hauser syndrome: a case report [PDF]
Journal of Medical Case ReportsBackground Herniation of female genital organs complicated by Mayer–Rokitansky–Küster–Hauser syndrome in adolescents is rarely reported in previous studies, and delayed diagnosis or misdiagnosis of this situation can lead to serious injury.
Weichao Liang +3 more
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Mayer Rokitansky Kuster Hauser Syndrome [PDF]
Andalas Obstetrics and Gynecology Journal, 2023 Mayer Rokitansky Küster Hauser syndrome (MRKH) is a syndrome characterized by uterine, cervix, and the two third of upper vagina aplasia which is the cause of incomplete development of the Müllerian duct.
Arga Kafi Perdana Kusuma +1 more
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Rectovaginal fistula in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]
Urology Case ReportsMRKH syndrome is defined by the congenital absence of the uterus and the upper two-thirds of the vagina in females, who otherwise exhibit normal secondary sexual characteristics and possess a typical 46, XX karyotype. Here we report a case of 23 year old
Puvvada Sandeep +4 more
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Rare Association of Mayer–Rokitansky–Kuster–Hauser Syndrome with Rectovestibular Fistula and Colonic Atresia [PDF]
Journal of Indian Association of Pediatric SurgeonsRectovestibular fistula is the most common presentation of female anorectal malformation. Its association with Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome and Colonic atresia is uncommon.
Audrey Pais +5 more
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A Novel Association of Colonic Duplication with Mayer–Rokitansky–Kuster–Hauser Syndrome in an Adolescent Girl [PDF]
Journal of Indian Association of Pediatric SurgeonsThe association is defined as two or more malformations with unclear relationships, which do not fit the criteria of a syndrome. This case report presents a rare finding of tubular colonic duplication in association with Mayer–Rokitansky–Küster–Hauser ...
Rajib Bora +4 more
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Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]
Revista Brasileira de Ginecologia e ObstetríciaClaudia Cristina Takano Novoa +2 more
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Hollow vaginal stent for a case of Mayer-Rokitansky-Kuster-Hauser syndrome: a case report
The Pan African Medical Journal, 2021 Congenital vaginal agenesis is a common condition with an instance of 1 in 5000 females. It is usually associated with Mayer-Rokitansky-Kuster Hauser syndrome. Such anomalies have a high impact on the physiology and psychology of patients.
Sharayu Vinod Nimonkar +1 more
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Mayer–Rokitansky–Küster–Hauser syndrome
Акушерство, гинекология и репродукция, 2023 The Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is an instructive story not only from a historical but also a gnoseological perspective. The mechanisms of embryogenesis as well as multiple aspects for correction of this syndrome remain enigmatic and ...
R. T. Adamyan +6 more
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