Cadaveric case report of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type II
Translational Research in AnatomyBackground: During a routine cadaver dissection, findings led to the recognition of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. MRKH is the second most common cause of primary amenorrhea in females.
Amanda Cobb, Cara L. Fisher
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Paraparesis and congenital severe hyperkyphosis in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: A rare deformity management during the Sars-Cov-2 pandemic [PDF]
Brain and Spine, 2023 Introduction: Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) syndrome can be classified into two types: type I (isolated) without extragenital abnormalities; type II (associated) with the presence of extragenital dimorphisms.
Giovanni Andrea La Maida +2 more
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Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility
Acta Obstetricia et Gynecologica ScandinavicaIntroduction Mayer‐Rokitansky‐Küster‐Hauser (MRKH) syndrome with utero‐vaginal aplasia is the most severe form of the Müllerian duct anomalies and can be associated with extra‐genital abnormalities such as renal or skeletal anomalies, hearing loss, or ...
Auriane Cospain +17 more
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MRKH syndrome: a review of literature [PDF]
International Journal of Reproduction, Contraception, Obstetrics and Gynecology, 2018 Primary amenorrhea is defined as failure to achieve menarche till age of 14 years in absence of normal secondary sexual characters or till 16 years irrespective of secondary sexual characters. The most common cause of primary amenorrhea is gonadal pathology followed by Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome).
Nidhi Jain, Jyotsna Harlalka Kamra
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Laparoscopic Davydov Procedure for Creation of Neovagina in MRKH Syndrome [PDF]
Bioscientia Medicina : Journal of Biomedicine and Translational Research, 2021 Introduction: The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a condition in which there is an absence of the uterus and the upper part (2/3) of the vagina. Women with MRKH syndrome show normal development of secondary sexual characteristics and a normal 46, XX karyotype. MRKH syndrome is a common cause of primary amenorrhea.
Ratih Krisna, null Rizky Agustria
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Isolated Mayer–Rokitansky–Kuster–Hauser syndrome (MRKH): Case Report
Andalas Obstetrics and Gynecology Journal, 2023 Background:Mayer–Rokitansky–Kuster–Hauser syndrome (MRKH) is a rare complex of congenital malformations characterized by aplasia of the uterus and upper (two-thirds) vagina in a woman with normal ovaries and fallopian tubes, secondary sexual ...
Eka Putri, Mondale Saputra
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Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome [PDF]
African Journal of Urology, 2013 Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina. Secondary sexual characteristics and karyotype are normal. This syndrome affects at least 1 out of 4500 women.
L.E. Mubenga +4 more
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Mayer–Rokitansky–Kuster–Hauser syndrome: Syndrome of Mullerian agenesis – A report of two cases
Medical Journal of Dr. D.Y. Patil University, 2017 The Mayer–Rokitansky–Kuster–Hauser syndrome (MRKH syndrome), simply called Rokitansky syndrome or vaginal aplasia of the uterus, is a congenital condition that is characterized by the absence of the uterus and vagina, but ovaries are present and the ...
Sushma Yalavarthi +3 more
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Mayer-Rokitansky-Küster-Hauser syndrome type II complicated by strangulated left inguinal ovarian-fallopian tube hernia in a pediatric patient: a case report [PDF]
BMC PediatricsBackground Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder characterized by Müllerian duct anomalies. Patients have a significantly higher incidence of inguinal hernia (6.4%-15.6%) compared to the general female population.
Hailong Su, Tingdong Yuan
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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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