Apert′s Syndrome: A Rare Case Report
Apert′s syndrome /Acrocephalosyndactyly is a rare, congenital disorder characterized by craniosynostosis, midfacial malformations and symmetrical syndactyly. It is caused by a genetic mutation in the FGFR2 gene on chromosome 10. Although the syndrome has typical clinical features, the relative rarit...
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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Medknow Publications
2010-01-01
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| coleção: | Journal of Indian Academy of Oral Medicine and Radiology |
| Assuntos: | |
| Acesso em linha: | http://www.jiaomr.in/article.asp?issn=0972-1363;year=2010;volume=22;issue=4;spage=232;epage=235;aulast=Dalal;type=0 |
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