All issues > Volume 33(11); 1990

Original Article

J Korean Pediatr Soc. 1990;33(11):1574-1578. Published online November 30, 1990.

A Case of Cloacal Exstrophy.

Kyung Hwan Oh¹, Joon Soo Park¹, Hak Joo Cha¹, Sang Jhoo Lee¹

¹Department of Pediatrics, College of Medicine, Soon Chun Hyang. University, Seoul, Korea

Received: August 13, 1990;  Accepted: September 28, 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.

Keywords :Cloacal Exstrophy