| CASE REPORT |
|
| Year : 2010 | Volume
: 1
| Issue : 4 | Page : 277-280 |
|
|
Familial Crouzon syndrome
Y Samatha1, T Harsha Vardhan1, A Ravi Kiran1, AJ Sai Sankar2, B Ramakrishna1
1 Department of Oral Medicine and Radiology, Sibar Institute of Dental Sciences, Guntur 522509, Andhra Pradesh, India
2 Department of Pedodontics, Sibar Institute of Dental Sciences, Guntur 522509, Andhra Pradesh, India
Correspondence Address:
Y Samatha
Department of Oral Medicine and Radiology, Sibar Institute of Dental Sciences, Guntur 522509, Andhra Pradesh
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0976-237X.76402
|
|
|
Crouzon syndrome is an autosomal dominant condition of the craniosynostotic syndromes without syndactyly and with various dentofacial anomalies. Craniosynostosis, maxillary hypoplasia, shallow orbits, ocular proptosis and hypertelorism are the characteristic features of Crouzon syndrome. This report describes the variable clinical features in affected individuals over two generations of a family with dentofacial deformities and review of literature. |
|
|
|
| [FULL TEXT] [PDF]* |
|
 |
|
