Clinical and Experimental Pediatrics

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Original Article

Kyung Hwan Oh, Joon Soo Park, Hak Joo Cha, Sang Jhoo Lee

Clin Exp Pediatr. 1990;33(11):1574-1578. Published online November 30, 1990

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.

A Case of Cloacal Extrophy.

Byung Ho Lee, Soon Seon Lim, Young Ha Kim, Moon Ki Cho

Clin Exp Pediatr. 1988;31(3):404-409. Published online March 31, 1988

Cloacal exstrophy is an extremly rare and curious anomaly that involves not only the genitourinary system but also the intestinal tract, resulted from the abnormaly large cloacal membrane and its early dehiscence. The authors experienced a case of cloacal exstrophy in one day old neonate whose intestine and bladder were exstrophied and showed omphalocele, imperforated anus and meningocele. Radiologic examination revealed widely separated symphysis pubic...

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