Pierre Robin sequence with H-type tracheoesophageal fistula and congenital heart disease
| Autor: | Erdal Peker, Keziban Bulan, Nihat Demir, Oğuz Tuncer, Lokman Üstyol |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
congenital
hereditary and neonatal diseases and abnormalities medicine.medical_specialty Robin Sequence Heart disease business.industry Glossoptosis Tracheoesophageal fistula medicine.disease Surgery Otorhinolaryngology Pediatrics Perinatology and Child Health medicine Congenital disease medicine.symptom Membranous Ventricular Septal Defect business |
| Zdroj: | International Journal of Pediatric Otorhinolaryngology Extra. 8:50-52 |
| ISSN: | 1871-4048 |
| DOI: | 10.1016/j.pedex.2013.02.003 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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