Frank ter Haar syndrome additional findings
Dentomaxillofacial Radiology, cilt.45, sa.2, ss.1-4, 2016 (Scopus)
- Yayın Türü: Makale / Vaka Takdimi
- Cilt numarası: 45 Sayı: 2
- Basım Tarihi: 2016
- Dergi Adı: Dentomaxillofacial Radiology
- Derginin Tarandığı İndeksler: Scopus
- Sayfa Sayıları: ss.1-4
- İstanbul Üniversitesi Adresli: Evet
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.