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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. |
