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Journal of Orthopedic Education

Volume  8, Issue 1, January-April 2022, Pages 23-25
 

Case Report

A Case Report Apert Syndrome

Supraja P1, Santhosh Kumar M2, Anitha C3

1Postgraduate, 2Associate Professor, 3Professor, Department of Pediatrics, JSS Medical College, JSS Academy of Higher Education and Research, Mysore 570015, Karnataka, India.

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DOI: http://dx.doi.org/10.21088/joe.2454.7956.8122.3

Abstract

 Apert syndrome (acrocephalosyndactyly) is an autosomal dominant disorder characterized by craniosynostosis, syndactyly, and midfacial malformation.

 Keywords: Possible mechanism of injury and operative procedures are discussed.

 

 


Corresponding Author : Santhosh Kumar M