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KIDNEY ON MAYER-ROKITANSKY-KÜSTER-HAUSER SYNDROME [PDF]

open access: yes, 2014
The Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) is a rare disorder characterized by congenital absence of upper part of the vagina and the absence or atresia of the uterus. The prevalence has been reported as one in 4000-5000 female births.
Breda, Giovanni Luis   +2 more
core   +1 more source

sj-docx-1-hpq-10.1177_13591053231199253 – Supplemental material for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

open access: yes, 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
core   +1 more source

Percutaneous closure of isolated ostium secundum-type atrial septal defect in a patient with Mayer-Rokitansky-Küster-Hauser syndrome

open access: yesRevista 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
doaj   +1 more source

sj-docx-3-hpq-10.1177_13591053231199253 – Supplemental material for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

open access: yes, 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

META-ANALYSIS : COMPARISON OF NEOVAGINA SUCCESS RATE WITH VECCHIETTI'S LAPAROSCOPIC METHOD AND DAVYDOV'S LAPAROSCOPIC METHOD IN MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME (MRKH) PATIENTS

open access: yesMedical 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
doaj   +1 more source

Vaginoplasty with oxidized cellulose in mayer–rokitansky–küster–hauser syndrome

open access: yesJournal 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
doaj   +1 more source

sj-docx-4-hpq-10.1177_13591053231199253 – Supplemental material for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

open access: yes, 2023
sj-docx-4-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

sj-docx-2-hpq-10.1177_13591053231199253 – Supplemental material for Issues of identity, perceptions and isolation: An interpretative phenomenological analysis of women’s experience of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

open access: yes, 2023
sj-docx-2-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

Gonadal Dysgenesis 46, XX Associated with Mayer-Rokitansky-Kuster-Hauser Syndrome: One Case Report

open access: yesObstetrics 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
doaj   +1 more source

Mayer-Rokitansky-Küster-Hauser syndrome

open access: yesJKS (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
doaj   +1 more source

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