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

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