Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report
DOI:
https://doi.org/10.21699/jns.v5i3.326Keywords:
Esophageal atresia, Anorectal malformation, Bowel duplication, Mullerian anomaliesAbstract
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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Published
2016-07-01
How to Cite
1.
Angotti R, Molinaro F, Bulotta AL, Ferrara F, Sica M, Bindi E, Messina M. Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report. J Neonatal Surg [Internet]. 2016Jul.1 [cited 2021Feb.28];5(3):32. Available from: https://jneonatalsurg.com/ojs/index.php/jns/article/view/299
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Case Report
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Copyright (c) 2016 Journal of Neonatal Surgery

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