Síndrome de Apert. Reporte de caso en odontopediatría
Apert syndrome accounts for 5% of all craniosynostosis syndromes and shows a prevalence of 1 in 60000 live births. Is one of the five craniosynostosis syndromes associated with single mutations in the Fibroblast Growth Factor Receptor 2 (FGF-R2) gene, with chromosomal localization at 10q26. The purp...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2011 |
| País: | Perú |
| Institución: | Universidad Nacional Mayor de San Marcos |
| Repositorio: | Revistas - Universidad Nacional Mayor de San Marcos |
| Idioma: | español |
| OAI Identifier: | oai:revistasinvestigacion.unmsm.edu.pe:article/2934 |
| Acceso en línea: | https://revistasinvestigacion.unmsm.edu.pe/index.php/odont/article/view/2934 |
| Access Level: | acceso abierto |
| Palabra clave: | Síndrome de Apert Craneosinostosis Gen del Receptor 2 del factor de crecimiento. Apert syndrome craniosynostosis Fibroblast growth factor receptor 2 gene. |
| Sumario: | Apert syndrome accounts for 5% of all craniosynostosis syndromes and shows a prevalence of 1 in 60000 live births. Is one of the five craniosynostosis syndromes associated with single mutations in the Fibroblast Growth Factor Receptor 2 (FGF-R2) gene, with chromosomal localization at 10q26. The purpose of this paper was to describe a case of Apert syndrome, show Pediatric dentistry managementand discuss their craniofacial features in an 8-year-old boy who presented Craniosynostosis, turribrachycephaly, syndactylies of the hands and feet, with multiple intraoral features. |
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