pyloric atresia-three cases and review of literature
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ID: 215601
2014
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Abstract
Pyloric atresia (PA) is a rare congenital anomaly that constitutes approximately 1% of all intestinal atresias, and its incidence is approximately 1 in 100,000 live births. PA may occur as an isolated condition or associated with other abnormalities, the most common being Junctional epidermolysis bullosa (JEB). Evidence suggests that PA-EB (Pyloric Atresia - Epidermolysis Bullosa) Syndrome is a distinct entity. In this report, we present three cases of pyloric atresia, one of which was associated with Junctional epidermolysis bullosa. The literature on the subject is also reviewed.
| Reference Key |
parelkar2014africanpyloric
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|---|---|
| Authors | ;Sandesh V Parelkar;Satish P Kapadnis;Beejal V Sanghvi;Prashant B Joshi;Dinesh Mundada;Shishira Shetty;Sanjay N Oak |
| Journal | intelligent systems reference library |
| Year | 2014 |
| DOI |
10.4103/0189-6725.143178
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| URL | |
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