Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare anomaly in women and is characterized by congenital aplasia of the uterus and vagina, with normal development of secondary sexual characteristics and a normal karyotype. We report a case of a 38-year-old women with MRKH syndrome that had experienced urethral sex for many years. She presented with urinary incontinence and dyspareunia. The ...

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by either isolated uterovaginal agenesis or associated with other organ anomalies in genetic women with normal development of secondary sexual characteristics. It affects at least 1 out of 4500 Women. We report an uncommonly seen unique sub type of MRKH syndrome, co-existing with imperforate anus and rectovaginal fistula (RVF) ...

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is rare congenital anomaly with complete absence of uterus and upper part vagina. Fibroids are one the most common benign tumours arising in women. from Mullerian remnants very rare. These fibroids often pose difficulty diagnosis management. Here, we report a case MRKH treatment provided for patient.

Background: The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the most common cause of uterine aplasia, with a worldwide frequency 1 in 4500 females. Although abundant literature present regarding different available methods for creating neovagina MRKH syndrome, attention dedicated to these women’s reproductive potential remains insufficient. Methods: Online searches were carried out PubMed...

INTRODUCTION The purpose of the study was to determine whether women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome differ from healthy women as regards personality traits and coping styles. MATERIAL AND METHODS Personality (the Big Five) and coping styles (problem-, emotion- and avoidance-focused coping) were analyzed in a group of 46 women with MRKH syndrome (age: M = 23.48; SD = 4.88)...

BACKGROUND Uterovaginal agenesis (Mayer-Rokitansky-Küster-Hauser Syndrome; MRKH) is a congenital nonformation of the vagina and the uterus, but with normal ovaries. OBJECTIVE The authors investigated the psychological impact of this disorder, about which very little is known. METHOD A group of 66 women with MRKH were compared with 31 control-group women on a range of self-rating scales asse...

Turner syndrome and Mayer-Rokitansky-Kuster-Hauser (MRKH) is a rare association. The incidences of MRKH syndromes are estimated at 1/2000 1/4500 female births respectively. This 23-year-old patient, born consanguineous marriage, who was referred to us for exploration primary amenorrhoea. karyotype, performed three times, from peripheral blood lymphocytes 45X0. diagnosis associated with retained.

BACKGROUND The Mayer-Rokitansky-Kuester-Hauser (MRKH) syndrome is a malformation of the female genitals (occurring in one in 4000 female live births) as a result of interrupted embryonic development of the Müllerian (paramesonephric) ducts. This retrospective study examined the issue of associated malformations, subtyping, and the frequency distribution of subtypes in MRKH syndrome. METHODS F...

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is one of the rare disorder of Mullerian agenesis leading to non-development of uterus and vagina. Its association with anorectal malformation is rare. We report a case of MRKH syndrome with recto-vestibular in a female child. The child had undergone a sigmoid loop colostomy in the neonatal period. On clinical examination of the perineum, a fistula...

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by uterine and vaginal canal aplasia in normal karyotype human females and is a syndrome with poorly defined etiology. Reproductive toxicity of phthalate esters (PEs) occurs in rat offspring exposed in utero, a phenomenon that is better studied in male offspring than females. The current study reports female reproductive tract malf...