Fig. 19.1
Diagrammatic representation of antral membrane (a) and antral membrane forming a windsock (b)
Rarely, there is an antral atresia with a gap (Fig. 19.2).

Fig. 19.2
Diagrammatic representation of antral gap atresia
Pyloric atresia is divided into three types:
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Type 1: Pyloric atresia with a membrane (Fig. 19.3a)Fig. 19.3a and b Diagrammatic representation of types 1and 2 pyloric atresia
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Type 2: Pyloric atresia with a solid cord between the two ends (Fig. 19.3b)
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Type 3: Pyloric atresia with a gap between the stomach and duodenum (Fig. 19.4)Fig. 19.4Diagrammatic representation of type 3 pyloric atresia
Type 1 is the commonest.
Associated Anomalies
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Epidermolysisbullosa (Fig. 19.5; the association of CPA with EB should not preclude surgical treatment).Fig. 19.5a and b Clinical photograph showing aplasia cutis congenita and epidermolysisbullosa in a patient with congenital pyloric atresia
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ACC.
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Hereditary multiple intestinal atresia (HMIA) .
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CPA in association with HMIA is universally fatal as so far none of the reported cases survived.
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Recently, a combined immunodeficiency syndrome was reported in patients with HMIA.
Presentation
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Recurrent nonbilious vomiting in a newborn.
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