Results 31 to 40 of about 1,400,939 (196)
Revista Portuguesa de Cardiologia, 2016 Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital anomaly characterized by complete or partial aplasia of the uterus and the upper part of the vagina. It is reported to be associated with cardiovascular disorders including atrial septal
Murat Akcay +4 more
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Medical and Health Science Journal, 2020 Background: Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKH) is caused by an embryological growth disorder of the mullerian duct. Laparoscopic Vecchietti and Davydov are laparoscopic surgery techniques that are often used for neovaginal surgery ...
Yanuar Prionggo +1 more
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Vaginoplasty with oxidized cellulose in mayer–rokitansky–küster–hauser syndrome
Journal of Indian Association of Pediatric Surgeons, 2021 Mayer–Rokitansky–Küster–Hauser syndrome (MRKHS) is the major cause of vaginal agenesis. Vaginoplasty with oxidized cellulose has been used by gynecologists as a surgical option in vaginal agenesis; however, it is not very widespread among pediatric ...
Mila Torii Corrêa Leite +2 more
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SAGE Open Medical Case Reports, 2019 The Mayer-Rokitansky-Küster-Hauser syndrome is the congenital absence or underdevelopment of the uterus and vagina even though the external genitalia, ovaries and ovarian function are normal. This condition is uncommon in Cameroon. A 23-year-old woman of
Thomas Obinchemti Egbe +4 more
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Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report
Journal of Medical Case Reports, 2010 Introduction We report the case of an unusual association of Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome. This association has never previously been reported in the medical literature.
Shukla Umesh +3 more
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Journal of Medical Case Reports, 2012 Introduction This case report describes an association between an exceptionally rare congenital anomaly and differentiated thyroid carcinoma. Mayer-Rokitansky-Küster-Hauser syndrome is characterized by vaginal aplasia associated with other Müllerian duct
Piciu Doina +2 more
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Prolapse and sexual function 8 years after neovagina according to Shears: a study of 43 cases with Mayer-von Rokitansky-Küster-Hauser syndrome [PDF]
, 2013 To investigate sexual and anatomical outcome after Shears neovagina in patients with Mayer-von Rokitansky-Kuster-Hauser syndrome (MRKH)
Im Obersteg, Jeannine +4 more
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Mayer-Rokitansky-Küster-Hauser syndrome
JKS (Jurnal Kedokteran Syiah Kuala), 2020 Abstrak. Mayer–Rokitansky–Küster–Hauser syndrome (MRKH) adalah suatu sindrom yang ditandai dengan aplasia uterus, serviks, dan 2/3 vagina bagian atas karena perkembangan yang tidak sempurna dari duktus Mullerian.
Cut Meurah Yeni +2 more
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Polymorphisms in DLGH1 and LAMC1 in Mayer–Rokitansky–Kuster–Hauser syndrome [PDF]
Reproductive BioMedicine Online, 2012 Müllerian agenesis, also termed the Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) is a disorder with an incidence of approximately 1 in 4500 newborn girls. This study screened 12 patients with MRKHS for mutations in two genes, LAMC1 and DLGH1, involved in the development of Müllerian structures and found 10 previously described variants and no novel ...
Celia, Ravel +5 more
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Journal of Nepal Medical Association, 2019 Gonadal dysgenesis is a rare genetically heterogeneous disorder characterized by underdeveloped ovaries with consequent, impuberism, primary amenorrhea, and hypergonadotropic hypogonadism .Mullerian agenesis or Mayer‑Rokitansky‑Kuster‑Hauser syndrome is ...
Santosh Kumar Jha +2 more
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