Congenital pyloric atresia: clinical features, diagnosis, associated anomalies, management and outcome

Conclusion: CPA is a very rare malformation that can be familial and inherited as an autosomal recessive. It can either occur as an isolated lesion with an excellent prognosis, or be associated with other anomalies. The overall prognosis of CPA, however, is still poor, and this is due to the frequent-and often fatal-associated anomalies.
Source: Annals of Pediatric Surgery - Category: Surgery Tags: Original Articles Source Type: research