Results 21 to 30 of about 262,079 (155)
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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Mayer Rokitansky Kuster Hauser Syndrome
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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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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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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Gonadal Dysgenesis 46, XX Associated with Mayer-Rokitansky-Kuster-Hauser Syndrome: One Case Report
Obstetrics and Gynecology International, 2010 Introduction. The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare and appears to be coincidental, independent of chromosomal anomalies. Case Report.
N. Bousfiha +5 more
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, 2023 sj-docx-1-hpq-10.1177_13591053231199253 for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome by Rebecca Gilfillan and Pelham Carter in ...
Rebecca Gilfillan (17070078) +1 more
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Estudio de caso: paciente femenina de 5 años de edad con síndrome de Mayer-Rokitansky-Küster-Mauser (MRKH). Citogen, Hospital Metropolitano. Quito - Ecuador [PDF]
, 2022 Determinar las características clínicas, genéticas, criterios diagnósticos, manejo integral y pronóstico de una paciente pediátrica con Síndrome de Mayer-Rokitansky-Küster-Hauser.
Medina Valencia, David Rafael
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, 2023 sj-docx-3-hpq-10.1177_13591053231199253 for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome by Rebecca Gilfillan and Pelham Carter in ...
Rebecca Gilfillan (17070078) +1 more
core +1 more source
Revista Colombiana de Obstetricia y Ginecología, 2013 Introducción: el síndrome de Mayer-Rokitansky-Küster-Hauser (SMRKH) es un espectro de anomalías de los conductos müllerianos caracterizado por la la ausencia congénita de útero y vagina en mujeres fenotípicamente normales, con cariotipo 46 XX, con un ...
Guillermo Páez-López +7 more
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, 2021 Introducción: La amenorrea es uno de los motivos más comunes en la atención primaria, donde el síndrome de Mayer-Rokitansky-Küster-Hauser se presenta como una anomalía congénita inusual del tracto genital.
Alvarez Mena, Cristian Enrique
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