Pierre Robin sequence with H-type tracheoesophageal fistula and congenital heart disease |
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| Authors: | Nihat Demir Erdal Peker Oğuz Tuncer Lokman Üstyol Keziban Bulan |
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| Affiliation: | 1. Universitat Autònoma de Barcelona, Department of Business, Edifici B, Campus UAB, 08913 Bellaterra, Barcelona, Spain;2. Fundación ECSIM, Medellín, Colombia;3. Deusto Business School, University of Deusto, Mundaiz 50, 20012 Donostia-San Sebastian, Spain;4. Universitat Autònoma de Barcelona, Tourism and Hotel Management School, Edifici Blanc, Campus UAB, 08913 Bellaterra, Barcelona, Spain;5. Universitat Oberta de Catalunya, Economics and Business Studies, Internet Interdisciplinary Institute (IN3), MediaTIC Building, Roc Boronat Street, 117, 6th Floor, 08018 Barcelona, Spain;1. University at Albany, State University of New York, 399 Social Sciences Building, 1400 Washington Avenue, Albany, NY 12222, United States;2. University of Notre Dame, 114-A Haggar Hall, Notre Dame, IN 46556, United States |
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| 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. |
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