Please use this identifier to cite or link to this item:
|Title:||Mayer-Rokitansky syndrome and anorectal malformation.|
|Authors:||Patankar, Shreeprasad P|
Patankar, Shilpa S
|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.|
|Appears in Collections:||Indian Journal of Pediatrics|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.