Apert syndrome.

Abstract

Apert syndrome (acrocephalosyndactyly) is a rare developmental malformation characterized by craniosynostosis, mid-face hypoplasia, symmetrical syndactyly of hands and feet. The prodromal characteristics for the typical cranio-facial appearance are early craniosynostosis of the coronal suture, cranial base and agenesis of the sagittal suture. The purpose of… (More)
DOI: 10.4103/0970-4388.76169

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Cite this paper

@article{Kannan2010ApertS, title={Apert syndrome.}, author={Vaidyanathan Kannan}, journal={Journal of the Indian Society of Pedodontics and Preventive Dentistry}, year={2010}, volume={28 4}, pages={322-5} }