Pierre Robin Sequence With H-Type Tracheoesophageal Fistula and Congenital Heart Disease
| dc.authorscopusid | 55598145000 | |
| dc.authorscopusid | 26025132600 | |
| dc.authorscopusid | 56186063400 | |
| dc.authorscopusid | 35243692700 | |
| dc.authorscopusid | 57189220861 | |
| dc.contributor.author | Demir, N. | |
| dc.contributor.author | Peker, E. | |
| dc.contributor.author | Tuncer, O. | |
| dc.contributor.author | Üstyol, L. | |
| dc.contributor.author | Bulan, K. | |
| dc.date.accessioned | 2025-05-10T16:59:59Z | |
| dc.date.available | 2025-05-10T16:59:59Z | |
| dc.date.issued | 2013 | |
| dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
| dc.department-temp | Demir N., YYU School of Medicine, Department of Pediatrics, Division of Neonatology, Van, Türkiye; Peker E., YYU School of Medicine, Department of Pediatrics, Division of Neonatology, Van, Türkiye; Tuncer O., YYU School of Medicine, Department of Pediatrics, Division of Neonatology, Van, Türkiye; Üstyol L., YYU School of Medicine, Department of Pediatrics, Division of Neonatology, Van, Türkiye; Bulan K., YYU School of Medicine, Department of Pediatrics, Division of Neonatology, Van, Türkiye | en_US |
| dc.description.abstract | Pierre 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. | en_US |
| dc.identifier.doi | 10.1016/j.pedex.2013.02.003 | |
| dc.identifier.endpage | 52 | en_US |
| dc.identifier.issn | 1871-4048 | |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.scopus | 2-s2.0-84875365383 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 50 | en_US |
| dc.identifier.uri | https://doi.org/10.1016/j.pedex.2013.02.003 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14720/4817 | |
| dc.identifier.volume | 8 | en_US |
| dc.identifier.wosquality | N/A | |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | International Journal of Pediatric Otorhinolaryngology Extra | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Pierre Robin Sequence | en_US |
| dc.subject | Tracheoesophageal Fistula | en_US |
| dc.subject | Ventricular Septal Defect | en_US |
| dc.title | Pierre Robin Sequence With H-Type Tracheoesophageal Fistula and Congenital Heart Disease | en_US |
| dc.type | Article | en_US |