A Case of Cloacal Exstrophy. |
Kyung Hwan Oh, Joon Soo Park, Hak Joo Cha, Sang Jhoo Lee |
Department of Pediatrics, College of Medicine, Soon Chun Hyang. University, Seoul, Korea |
총배출강 외번증 1례* |
오경환, 박준수, 차학주, 이상주 |
순천향대학교 의과대학 소아과학교실 |
Received: 13 August 1990 • Accepted: 28 September 1990 |
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Abstract |
Cloacal exstrophy is a rare congenital anomaly. This anomaly results from failure of cloacal
cpntatinn with the persistence of ? into which ilpiiir* and a rndirnAntary
hind gut open. We have experienced in a 1-day old male neonate a typical case of cloacal exstrophy
associated with omphalocele, genital anomaly, imperforated anus, meningocele, spina bifida, widely
separated symphysis and equinovarus.
A brief review of related literatures was made. |
Key Words:
Cloacal Exstrophy |
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