Abstract
Congenital pyloric atresia (CPA) is a very rare surgical condition which occurs in about 1 in 100,000 newborns [1]. usually seen as an isolated anomaly or be associated with other anomalies like epidermolysis bullosa [2]. It affects male and female patients equally. Therapeutic strategies are multiple. We emphasize the importance of a prompt diagnosis to avoid potentially fatal complications and to warrant a good outcome even in the presence of a strange form of PA in the neonatal period. We present an additional case managed at the department of pediatric surgery Mohamed V Hospital, Tangier.
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