Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis

Ozkan K. U., ÇOBAN Y. K., Uzel M., ERGÜN M. A., Oksuz H.

CLEFT PALATE-CRANIOFACIAL JOURNAL, cilt.43, sa.3, ss.317-320, 2006 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 43 Sayı: 3
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1597/05-032r1.1
  • Dergi Adı: CLEFT PALATE-CRANIOFACIAL JOURNAL
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.317-320
  • Gazi Üniversitesi Adresli: Evet

Özet

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.