A Case of Mayer-Rokitansky-K ster-Hauser(MRKH) Syndrome with Imperforate Anus and Unilateral Renal Agenesis
Journal of the Korean Society of Pediatric Nephrology
;
: 233-237, 2006.
Artículo
en Coreano
| WPRIM
| ID: wpr-206553
ABSTRACT
The clinical features of the Mayer-Rokitansky-K ster-Hauser(MRKH) syndrome include normal female secondary sex characteristics, normal genitalia, congenital absence of vagina, rudimentary or bipartite uterus, normal ovarian function and normal ovulation, 46, XX, karyotype, frequent association of renal, skeletal and other congenital anomalies. We experienced a case of a premature infant with MRKH syndrome who had imperforate anus and unilateral renal agenesis.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Ano Imperforado
/
Ovulación
/
Útero
/
Vagina
/
Recien Nacido Prematuro
/
Caracteres Sexuales
/
Cariotipo
/
Genitales
Límite:
Femenino
/
Humanos
/
Recién Nacido
Idioma:
Coreano
Revista:
Journal of the Korean Society of Pediatric Nephrology
Año:
2006
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS