Please use this identifier to cite or link to this item: http://imsear.hellis.org/handle/123456789/82598
Title: Mayer-Rokitansky syndrome and anorectal malformation.
Authors: Patankar, Shreeprasad P
Kalrao, Vijay
Patankar, Shilpa S
Issue Date: 5-Dec-2004
Citation: Patankar SP, Kalrao V, Patankar SS. Mayer-Rokitansky syndrome and anorectal malformation. Indian Journal of Pediatrics. 2004 Dec; 71(12): 1133-5
Abstract: Mayer Rokitansky Kuster Houser syndrome (MRKH syndrome) is characterized by Mullerian duct structures agenesis, vaginal atresia being the commonest variant. It can be associated with renal, skeletal, spine and other malformations. Patient with Mayer Rokitansky syndrome has a varied presentation from newborn period to adolescence. Thorough investigations are required for classification of the syndrome and diagnosis of associated anomalies. The MRKH syndrome patient may require complex vaginal reconstructive surgery and a detailed counseling about the potentials of menstruation and fertility. Here we are presenting a patient having association of anorectal malformation, Mullerian duct agenesis and renal anomaly.
URI: http://imsear.hellis.org/handle/123456789/82598
Appears in Collections:Indian Journal of Pediatrics

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