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

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Abstract

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.

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