Mayer-Rokitansky-Küster-Hauser Syndome and Laparoscopic Assisted Creation of Neovagina (Modified Vecchietti)
نویسندگان
چکیده
منابع مشابه
Mayer-rokitansky-küster-hauser Syndome and Laparoscopic Assisted Creation of Neovagina (modified Vecchietti)
Objective: To report the post operative 6 month results of tree patients with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome who underwent laparoscopic assisted creation of neovagina (Modified Vecchietti) by using "Neovagina Set" for the first time in our clinic. Design: Prospective evaluation. Setting: University hospital Patients: Three patients with MHRK syndrome. Interventions: Laparoscopic...
متن کاملSexual Life of Women With Mayer-Rokitansky-Küster-Hauser Syndrome After Laparoscopic Vecchietti Vaginoplasty
INTRODUCTION Adequate anatomic and physiologic functions of the genitalia are fundamental prerequisites for sexual well-being and reproduction. Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) compromises female sexual life and makes reproduction impossible. AIM To assess the psychosexual effect of vaginal reconstruction using the laparoscopic Vecchietti technique in patients with MRKHS. MET...
متن کاملEfficacy risks of the minimal-invasive plastic and reconstructive neovagina Vecchietti technique in Mayer-Rokitansky-Küster-Hauser syndrome
INTRODUCTION Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital disorder clinically defined by primary amenorrhea and infertility, congenital aplasia of the uterus and upper vagina. The patients with MRKH-syndrome have a female karyotype (46, XX), normally functioning ovaries and regular development of secondary sexual characters. Generally, the initial clinical sign of the syndrome...
متن کاملMayer-Rokitansky-Küster-Hauser (MRKH) syndrome
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. It affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently associated with renal, vertebral, and, to a lesser ext...
متن کاملCreation of a neovagina according to Wharton-Sheares-George in patients with Mayer-Rokitansky-Küster-Hauser syndrome.
OBJECTIVE To introduce a simple and quick surgical alternative for creating a neovagina in patients with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome that offers good anatomic and functional results. DESIGN Historical report. SETTING Tertiary center for gynecologic endocrinology. PATIENT(S) Three patients with MRKH syndrome. INTERVENTION(S) The creation of a neovagina according to Wha...
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ژورنال
عنوان ژورنال: Journal of Turkish Society of Obstetric and Gynecology
سال: 2013
ISSN: 1307-699X
DOI: 10.5505/tjod.2013.24392