Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report

Rossella Angotti, Francesco Molinaro, Anna Lavinia Bulotta, Francesco Ferrara, Marina Sica, Edoardo Bindi, Mario Messina

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.


Keywords


Esophageal atresia; Anorectal malformation; Bowel duplication; Mullerian anomalies

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DOI: http://dx.doi.org/10.21699/jns.v5i3.326

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