Sexual Response in Women With Mayer-Rokitansky-Küster-Hauser Syndrome With a Nonsurgical Neovagina

(Abstracted from Am J Obstet Gynecol 2018;219:283.e1–283.e8)Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an uncommon congenital condition characterized by an agenesis or hypoplasia of vagina and uterus. The first-line treatment approach—nononsurgical vaginal elongation by dilation—has high succ...

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Veröffentlicht in:Obstetrical & gynecological survey 2018-12, Vol.73 (12), p.692-693
Hauptverfasser: Both, Stephanie, Kluivers, Kirsten, ten Kate-Booij, Marianne, Weijenborg, Philomeen
Format: Artikel
Sprache:eng
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Zusammenfassung:(Abstracted from Am J Obstet Gynecol 2018;219:283.e1–283.e8)Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an uncommon congenital condition characterized by an agenesis or hypoplasia of vagina and uterus. The first-line treatment approach—nononsurgical vaginal elongation by dilation—has high success rates (90%–96%).
ISSN:0029-7828
1533-9866
DOI:10.1097/OGX.0000000000000629