International Journal of Clinical Pediatric Dentistry

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VOLUME 5 , ISSUE 3 ( September-December, 2012 ) > List of Articles

CASE REPORT

Apert Syndrome: A Case Report

Saba Khan, Laxmikanth Chatra, Prashanth Shenai, KM Veena

Keywords : Apert\'s, Symmetric, Syndactyly, Craniosynostosis, Acrocephalosyndactylia, Midface hypoplasia

Citation Information : Khan S, Chatra L, Shenai P, Veena K. Apert Syndrome: A Case Report. Int J Clin Pediatr Dent 2012; 5 (3):203-206.

DOI: 10.5005/jp-journals-10005-1166

License: CC BY-NC 4.0

Published Online: 01-12-2012

Copyright Statement:  Copyright © 2012; The Author(s).


Abstract

Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation and symmetrical syndactyly. We present a 10-month-old infant having all the features of classical Apert syndrome. How to cite this article: Khan S, Chatra L, Shenai P, Veena KM. Apert Syndrome: A Case Report. Int J Clin Pediatr Dent 2012; 5(3):203-206.


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