Diagnóstico Prenatal de síndrome de Apert

  1. Fernández Crespo, Blanca
  2. Silva, María da
  3. Benítez, Gidder
  4. Rumbao, Fabio
  5. Arcia, Orlando
  6. Hernández, Carlos
Revista:
Vitae: Academia Biomédica Digital

ISSN: 1317-987X

Año de publicación: 2002

Número: 13

Tipo: Artículo

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Otras publicaciones en: Vitae: Academia Biomédica Digital

Resumen

Apert 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.

Fuente de los datos: Dialnet