: 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.
Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report / Angotti, R; Molinaro, F; Bulotta, A L; Ferrara, F; Sica, M; Bindi, E; Messina, M. - In: JOURNAL OF NEONATAL SURGERY. - ISSN 2226-0439. - 5:3(2016), p. 32. [10.21699/jns.v5i3.326]