Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Añadir filtros








Intervalo de año
1.
Indian J Hum Genet ; 2011 May; 17(2): 48-53
Artículo en Inglés | IMSEAR | ID: sea-138934

RESUMEN

Craniosynsostosis syndromes exhibit considerable phenotypic and genetic heterogeneity. Sagittal synostosis is common form of isolated craniosynostosis. The sutures involved, the shape of the skull and associated malformations give a clue to the specific diagnosis. Crouzon syndrome is one of the most common of the craniosynostosis syndromes. Apert syndrome accounts for 4.5% of all craniosynostoses and is one of the most serious of these syndromes. Most syndromic craniosynostosis require multidisciplinary management. The following review provides a brief appraisal of the various genes involved in craniosynostosis syndromes, and an approach to diagnosis and genetic counseling.


Asunto(s)
Acrocefalosindactilia/epidemiología , Acrocefalosindactilia/genética , Niño , Suturas Craneales/anomalías , Craneosinostosis/epidemiología , Craneosinostosis/genética , Humanos , Hidrocefalia/epidemiología , Hidrocefalia/genética , Plagiocefalia/genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA