1.
Ann Card Anaesth
;
2011 Jan; 14(1): 62-65
Artículo
en Inglés
| IMSEAR
| ID: sea-139569
2.
Indian J Pediatr
;
2004 Dec; 71(12): 1133-5
Artículo
en Inglés
| IMSEAR
| ID: sea-82598
RESUMEN
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.
Asunto(s)
Anomalías Múltiples/diagnóstico , Canal Anal/anomalías , Huesos/anomalías , Niño , Femenino , Humanos , Riñón/anomalías , Conductos Paramesonéfricos/anomalías , Recto/anomalías , Síndrome , Vagina/anomalías
3.
Indian Pediatr
;
2004 May; 41(5): 511
Artículo
en Inglés
| IMSEAR
| ID: sea-10649