Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis

ÖZKAN K. U., ÇOBAN Y. K., Uzel M., Ergun M., Oksuz H.

Cleft Palate-Craniofacial Journal, vol.43, no.3, pp.317-320, 2006 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 43 Issue: 3
  • Publication Date: 2006
  • Doi Number: 10.1597/05-032r1.1
  • Journal Name: Cleft Palate-Craniofacial Journal
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.317-320
  • Keywords: Congenital radioulnar synostosis, Esophageal atresia, Pierre Robin sequence
  • Kocaeli University Affiliated: Yes


A wide spectrum of anomalies can be associated with Pierre Robin sequence. This report presents a 3-day-old infant with micrognathia, U-shaped cleft palate, low-set right ear with microtia, glossoptosis, esophageal atresia, and right congenital radioulnar synostosis. The association of congenital radioulnar synostosis and esophageal atresia with Pierre Robin sequence has not been previously described.