Demir, N.Peker, E.Tuncer, O.Üstyol, L.Bulan, K.2025-05-102025-05-1020131871-404810.1016/j.pedex.2013.02.0032-s2.0-84875365383https://doi.org/10.1016/j.pedex.2013.02.003https://hdl.handle.net/20.500.14720/4817Pierre Robin sequence (PRs) is a congenital disease characterized by micrognathia, cleft palate, glossoptosis and a wide range of other anomalies. The treatment of patients with PRs may be problematic due to the varying anomalies and high mortality rate. In this case report, a 1-day-old newborn with micrognathia, cleft lip and palate, glossoptosis, a membranous ventricular septal defect and an H-type tracheoesophageal fistula has been evaluated and discussed considering the current literature. To the best of our knowledge, the coexistence of PRs with a membranous ventricular septal defect and H-type tracheoesophageal fistula has not been previously described. © 2013 Elsevier Ireland Ltd.eninfo:eu-repo/semantics/closedAccessPierre Robin SequenceTracheoesophageal FistulaVentricular Septal DefectArticle82N/AN/A5052