Mayer Rokitansky Kuster Hauser syndrome with urogenital sinus anomaly
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2007; 17 (1): 57-58
en Inglés
| IMEMR
| ID: emr-83232
ABSTRACT
Mayer Rokitansky Kuster Hauser [MRKH] syndrome is a rare disorder, characterized by the congenital absence of uterus and associated renal tract anomalies. The case presented with primary amenorrhea and primary infertility, despite development of normal female secondary sexual characteristics. CT scan revealed absent uterus, a solitary left sided pelvic kidney and a vesicovaginal communication that, on cystoscopy, revealed urogenital sinus anomaly manifesting as a common channel formed due to absent anterior wall of vagina and posterior wall of urethra. The urogenital sinus anomaly in MRKH syndrome has not been reported earlier
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Síndrome
/
Anomalías Múltiples
/
Tomografía Computarizada por Rayos X
/
Fístula Vesicovaginal
/
Conductos Paramesonéfricos
Tipo de estudio:
Informe de Casos
Límite:
Femenino
/
Humanos
Idioma:
Inglés
Revista:
J. Coll. Physicians Surg. Pak.
Año:
2007
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