Rate the Article: The Mayer-Rokitansky-K'ster-Hauser (MRKH) Syndrome Associated with Anorectal Malformation ? Rectovaginal Fistula; A Rare Combination: Case Report, IJSR, Call for Papers, Online Journal
International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064

Downloads: 120 | Views: 325

Case Studies | Medicine Science | India | Volume 3 Issue 5, May 2014 | Rating: 6.1 / 10


The Mayer-Rokitansky-K'ster-Hauser (MRKH) Syndrome Associated with Anorectal Malformation ? Rectovaginal Fistula; A Rare Combination: Case Report

Shivaprakash Sosale. C, C. S. Ravikiran, R. Sujatha


Abstract: The Mayer-Rokitansky-Kster-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) in a 13 year old adolescent girl presented with passage of stool through introitus. We have discussed in brief the management including vaginal reconstructive surgery and detailed counseling regarding the potentials of coitus and fertility issues


Keywords: Anorectal malformation, Mullarian agenesis, Mayer-Rokitansky- Kster -Hauser syndrome, Rectovaginal fistula, Vaginal agenesis


Edition: Volume 3 Issue 5, May 2014,


Pages: 447 - 449



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