Seyrek görülen bir karin ön duvari defekti: Kloakal ekstrofi, omfalosel, anal atrezi

Persistent cloaca and cloacal exstrophy are the rare congenital anomalies of the urogenital system and anorectum. The persistent cloaca is formed by the rectum, vagina, and urethra approaching a common channel, resulting in the opening of a single perineal region. It is characterized by the exstrophy of the urinary tract, genital organs, and intestines as a result of inadequate closure of the abdominal wall. In this article, a newborn with cloacal exstrophy and omphalocele, diagnosed in prenatal period, was presented and discussed in the light of recent literature data.