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In recent decades, diagnosis of neonatal malformations has shown growing success thanks to advances in ultrasound diagnostics. Intra-abdominal cystic formation can be successfully diagnosed prenatally, most often in the third trimester, mainly as isolated unilateral lesions in otherwise healthy fetus. With the existence of intra-abdominal cyst in neonate, it is necessary to exclude urinary tract anomalies and abnormalities of the heart and the spine. We present diagnostic procedure and perinatal outcome of a female newborn with enteric duplication cyst.