Frank-ter Haar syndrome-additional findings?

Kose T. E. , Isler C., ŞENEL Ş. N. , Sitilci T., ÖZCAN İ., Aksakalli N.

DENTOMAXILLOFACIAL RADIOLOGY, cilt.45, sa.2, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45 Konu: 2
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1259/dmfr.20150119


Frank-ter Haar syndrome is a genetic disease that is transmitted by autosomal recessive pattern with characteristic features such as megalocornea or glaucoma, a prominent coccyx, heart defects, developmental delays, brachycephaly, a wide anterior fontanel, finger flexion deformities, full cheeks and micrognathia. Dentomaxillofacial features of this syndrome are not well documented in the literature. We present of a 21-year-old male with Frank-ter Haar syndrome and some features that may be linked with this syndrome not reported before in the literature.