Abstract
Congenital pyloric atresia is a very rare condition. Commonly, congenital pyloric atresia occurs as an isolated lesion, which has an excellent prognosis, but it can also be seen in association with other malformations, which can have a negative impact on the final outcome. The classification, clinical features and management are discussed.
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Further Reading
Al-Salem AH. Congenital pyloric atresia and associated anomalies. Pediatr Surg Int. 2007;23(6):559–63.
Al-Salem A, Nawaz A, Matta H, Jacobsz A. Congenital pyloric atresia: the spectrum. Int Surg. 2002;87:147–51.
Bass J. Pyloric atresia associated with multiple intestinal atresias and immune deficiency. J Pediatr Surg. 2002;37:941–2.
Ilce Z, Erdogan E, Kara C, Celayir S, Sarimurat N, Senyüz OF, et al. Pyloric atresia: 15-year review from a single institution. J Pediatr Surg. 2003;38:1581–4.
Moore CM. Congenital gastric outlet obstruction. J Pediatr Surg. 1989;24:1241–6.
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Al-Salem, A.H. (2020). Congenital Gastric Outlet Obstruction. In: Atlas of Pediatric Surgery. Springer, Cham. https://doi.org/10.1007/978-3-030-29211-9_47
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DOI: https://doi.org/10.1007/978-3-030-29211-9_47
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