Apert's syndrome: A rare case

Apert's syndrome: A rare case

Apert's syndrome is a rare type I acrocephalosyndactyly syndrome characterized by craniosynostosis, severe syndactyly of the hands and feet, and dysmorphic facial features. The purpose of this report is to present an Apert's syndrome patient by highlighting the craniofacial characteristics...

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Bibliographic Details
Main Authors: Tarun Kumar, Neha Arora, Gagan Puri, Aravinda Konidena
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Journal of Indian Academy of Oral Medicine and Radiology
Subjects:
Apert's syndrome
facial features
oral care
Online Access:http://www.jiaomr.in/article.asp?issn=0972-1363;year=2016;volume=28;issue=1;spage=83;epage=85;aulast=Kumar

Internet

http://www.jiaomr.in/article.asp?issn=0972-1363;year=2016;volume=28;issue=1;spage=83;epage=85;aulast=Kumar

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