Familial Crouzon syndrome
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...
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2010-01-01
|
| Series: | Contemporary Clinical Dentistry |
| Subjects: | |
| Online Access: | http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=4;spage=277;epage=280;aulast=Samatha |
| _version_ | 1811243237485051904 |
|---|---|
| author | Y Samatha T Harsha Vardhan A Ravi Kiran A J Sai Sankar B Ramakrishna |
| author_facet | Y Samatha T Harsha Vardhan A Ravi Kiran A J Sai Sankar B Ramakrishna |
| author_sort | Y Samatha |
| collection | DOAJ |
| description | 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. |
| first_indexed | 2024-04-12T14:03:57Z |
| format | Article |
| id | doaj.art-0d2bcd14355f4034834155bf7dc2398e |
| institution | Directory Open Access Journal |
| issn | 0976-237X 0976-2361 |
| language | English |
| last_indexed | 2024-04-12T14:03:57Z |
| publishDate | 2010-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Contemporary Clinical Dentistry |
| spelling | doaj.art-0d2bcd14355f4034834155bf7dc2398e2022-12-22T03:30:08ZengWolters Kluwer Medknow PublicationsContemporary Clinical Dentistry0976-237X0976-23612010-01-011427728010.4103/0976-237X.76402Familial Crouzon syndromeY SamathaT Harsha VardhanA Ravi KiranA J Sai SankarB RamakrishnaCrouzon 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.http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=4;spage=277;epage=280;aulast=SamathaCraniosynostosisCrouzon syndromedentofacial anomalies |
| spellingShingle | Y Samatha T Harsha Vardhan A Ravi Kiran A J Sai Sankar B Ramakrishna Familial Crouzon syndrome Contemporary Clinical Dentistry Craniosynostosis Crouzon syndrome dentofacial anomalies |
| title | Familial Crouzon syndrome |
| title_full | Familial Crouzon syndrome |
| title_fullStr | Familial Crouzon syndrome |
| title_full_unstemmed | Familial Crouzon syndrome |
| title_short | Familial Crouzon syndrome |
| title_sort | familial crouzon syndrome |
| topic | Craniosynostosis Crouzon syndrome dentofacial anomalies |
| url | http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=4;spage=277;epage=280;aulast=Samatha |
| work_keys_str_mv | AT ysamatha familialcrouzonsyndrome AT tharshavardhan familialcrouzonsyndrome AT aravikiran familialcrouzonsyndrome AT ajsaisankar familialcrouzonsyndrome AT bramakrishna familialcrouzonsyndrome |