More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalities which had not yet described in literature.
Angotti, R., Molinaro, F., Bulotta, A.L., Ferrara, F., Sica, M., Bindi, E., et al. (2016). Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report. JOURNAL OF NEONATAL SURGERY, 5(3), 32 [10.21699/jns.v5i3.326].
Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report
Angotti, R;MOLINARO, FRANCESCO;MESSINA, MARIO
2016-01-01
Abstract
More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalities which had not yet described in literature.
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https://hdl.handle.net/11365/1000490
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