Journal of the Korean Pediatric Society 1990;33(11):1574-1578.
Published online November 30, 1990.
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
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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