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- W79684736 abstract "espanolEl Sindrome de Apert es un trastorno autosomico dominante, caracterizado por craneosinostosis, hipoplasia del tercio medio de la cara y sindactilia de manos y pies. Presentamos un caso diagnosticado a las 24 semanas de gestacion, despues de realizar un ecosonograma en el cual se observaron las alteraciones caracteristicas. El diagnostico se confirmo al momento del nacimiento. Se realiza una revision y analisis de la literatura sobre el tema. EnglishApert syndrome is an autosomal dominant disorder characterized by craniosynostosis, midfacial malformations and symmetric syndactyly of hands and feet. We present a prenatal diagnosis at 24 weeks? gestation after sonography showing features deformity. The diagnosis was confirmed at birth. We present a review of the current literature regarding Apert syndrome." @default.
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- W79684736 date "2002-01-01" @default.
- W79684736 modified "2023-09-26" @default.
- W79684736 title "Diagnóstico Prenatal de síndrome de Apert" @default.
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