Frank-ter Haar syndrome--additional findings?


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

Dento maxillo facial radiology, vol.45, no.2, pp.20150119, 2016 (Journal Indexed in SCI Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 45 Issue: 2
  • Publication Date: 2016
  • Doi Number: 10.1259/dmfr.20150119
  • Title of Journal : Dento maxillo facial radiology
  • Page Numbers: pp.20150119
  • Keywords: Frank-ter Haar syndrome, paranasal sinus, impacted teeth, ETHMOID SINUS HYPOPLASIA, MAXILLARY, APLASIA

Abstract

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.