Frank-ter Haar syndrome--additional findings?
Dentomaxillofac Radiol
; 45(2): 20150119, 2016.
Article
de En
| MEDLINE
| ID: mdl-26582053
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.
Mots clés
Texte intégral:
1
Collection:
01-internacional
Base de données:
MEDLINE
Sujet principal:
Ostéochondrodysplasies
/
Malformations crâniofaciales
/
Cardiopathies congénitales
Type d'étude:
Diagnostic_studies
Limites:
Adult
/
Humans
/
Male
Langue:
En
Journal:
Dentomaxillofac Radiol
Année:
2016
Type de document:
Article
Pays d'affiliation:
Turquie