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Apert Syndrome: A Case Report

JOURNAL TITLE: International Journal of Clinical Pediatric Dentistry

Author

1. KM Veena
2. Saba Khan
3. Prashanth Shenai
4. Laxmikanth Chatra

ISSN

0974-7052

DOI

10.5005/jp-journals-10005-1166

Volume

Issue

Publishing Year

2012

Pages

Author Affiliations

Department of Oral Medicine and Radiology, Yenepoya Dental College and Hospital, Mangalore, Karnataka, India

Department of Oral Medicine and Radiology Yenepoya Dental College, Yenepoya University, Mangalore, Karnataka India

Department of Oral Medicine and Radiology, Yenepoya Dental College and Hospital Yenepoya University, Manglore, Karnataka, India

Article keywords

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

Abstract

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.