Frank-ter Haar syndrome--additional findings?
Dento maxillo facial radiology, cilt.45, sa.2, ss.20150119, 2016 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 45 Sayı: 2
- Basım Tarihi: 2016
- Doi Numarası: 10.1259/dmfr.20150119
- Dergi Adı: Dento maxillo facial radiology
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.20150119
- Anahtar Kelimeler: Frank-ter Haar syndrome, paranasal sinus, impacted teeth, ETHMOID SINUS HYPOPLASIA, MAXILLARY, APLASIA
- Recep Tayyip Erdoğan Üniversitesi Adresli: Hayır
Özet
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.