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Korean Journal of Obstetrics & Gynecology 1999;42(7):1577-1581.
Published online January 1, 2001.
A Case of Imperforate Cloacal Membrane Diagnosed by Autopsy.
S S Seo, G S Lim, J H Yeom, H S Lee, J G Chi, S H Kim
Abstract
Cloacal anomalies are very rare congenital malformations with the incidence of 1/50,000~250,000 births. Because of wide spectrum of abnormal anatomy involving urogenital and gastrointestinal systems, prenatal diagnosis is difficult. We present a case of cloacal anomaly which was initially presented as a fetal growing abdominal cyst. The cyst was spontaneously ruptured, and diagnosed as imperforate cloacal membrane at autopsy after preterm delivery.
Key Words: Cloacal anomaly, Fetal abdominal cyst, Imperforate cloacal membrane


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