Familial Crouzon syndrome
| Autor: | A Ravi Kiran, AJ Sai Sankar, T Harsha Vardhan, B Ramakrishna, Yalamanchili Samatha |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2010 |
| Předmět: |
Orthodontics
musculoskeletal diseases congenital hereditary and neonatal diseases and abnormalities Maxillary hypoplasia business.industry Crouzon syndrome Case Report Shallow orbits medicine.disease dentofacial anomalies Craniosynostosis lcsh:RK1-715 Dentofacial Deformity Ocular proptosis lcsh:Dentistry medicine Periodontics Syndactyly Oral Surgery Hypertelorism medicine.symptom business |
| Zdroj: | Contemporary Clinical Dentistry Contemporary Clinical Dentistry, Vol 1, Iss 4, Pp 277-280 (2010) |
| ISSN: | 0976-2361 0976-237X |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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