Mayer-Rokitansky syndrome and anorectal malformation.
Indian J Pediatr
;
2004 Dec; 71(12): 1133-5
Artigo
em Inglês
| IMSEAR
| ID: sea-82598
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.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Canal Anal
/
Reto
/
Síndrome
/
Vagina
/
Anormalidades Múltiplas
/
Osso e Ossos
/
Feminino
/
Humanos
/
Criança
/
Rim
Idioma:
Inglês
Revista:
Indian J Pediatr
Ano de publicação:
2004
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS