Pyloric atresia-Three cases and review of literature
Autor: | Sandesh V Parelkar, Satish P Kapadnis, Beejal V Sanghvi, Prashant B Joshi, Dinesh Mundada, Shishira Shetty, Sanjay N Oak |
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Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: | |
Zdroj: | African Journal of Paediatric Surgery, Vol 11, Iss 4, Pp 362-365 (2014) |
Druh dokumentu: | article |
ISSN: | 0189-6725 0974-5998 |
DOI: | 10.4103/0189-6725.143178 |
Popis: | 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. |
Databáze: | Directory of Open Access Journals |
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