1.
Ann Card Anaesth
;
2011 Jan; 14(1): 62-65
Artigo
em Inglês
| IMSEAR
| ID: sea-139569
2.
Indian J Pediatr
;
2004 Dec; 71(12): 1133-5
Artigo
em Inglês
| IMSEAR
| ID: sea-82598
RESUMO
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.
Assuntos
Anormalidades Múltiplas/diagnóstico , Canal Anal/anormalidades , Osso e Ossos/anormalidades , Criança , Feminino , Humanos , Rim/anormalidades , Ductos Paramesonéfricos/anormalidades , Reto/anormalidades , Síndrome , Vagina/anormalidades
3.
Indian Pediatr
;
2004 May; 41(5): 511
Artigo
em Inglês
| IMSEAR
| ID: sea-10649