Pregnancy in a case of Mayer-Rokitansky-Küster-Hauser Syndrome Gravidez num caso de Síndrome Mayer-Rokitansky-Küster-Hauser
نویسندگان
چکیده
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome refers to the congenital absence of the upper part (2/3) of the vagina with variable uterine development. In this disorder, infertility may be the most difficult aspect for the patient to accept. This review will describe a rare case of pregnancy in a woman with MRKH syndrome through assisted reproductive
منابع مشابه
The Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome Associated with Anorectal Malformation – Rectovaginal Fistula; A Rare Combination: Case Report
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) ...
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Introduction: The Mayer-Rokitansky-Küster-Hauser syndrome is characterized by the absence of the vagina and uterus and primary amenorrhea. Objective: The diagnostic evaluation and the therapeutic possibilities of a rare syndrome. Materials and methods: We present a case of a Rokitansky syndrome. Results: The patient presented normal development of secondary sexual characters. Analysis also show...
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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...
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Mayer-rokitansky-küster-hauser Syndome and Laparoscopic Assisted Creation of Neovagina (modified Vecchietti)
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