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KIDNEY ON MAYER-ROKITANSKY-KÜSTER-HAUSER SYNDROME [PDF]
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
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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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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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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
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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
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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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
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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
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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Mayer-Rokitansky-Küster-Hauser syndrome
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

