Apert syndrome: A rare anomalad

Apert syndrome: A rare anomalad

Apert syndrome is a developmental malformation characterized by craniosynostosis, a cone shaped calvarium, midface hypoplasia, pharyngeal attenuation, ocular manifestations and syndactyly of the hands and feet. The complex craniofacial and systemic deformities seen in Apert syndrome mandate a multid...

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Bibliographic Details
Main Authors: Himanshi Aggarwal, Saumyendra Vikram Singh, Pradeep Kumar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:CHRISMED Journal of Health and Research
Subjects:
Apert syndrome
apertognathia
craniosynostosis
syndactyly
Online Access:http://www.cjhr.org/article.asp?issn=2348-3334;year=2014;volume=1;issue=3;spage=206;epage=208;aulast=Aggarwal

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http://www.cjhr.org/article.asp?issn=2348-3334;year=2014;volume=1;issue=3;spage=206;epage=208;aulast=Aggarwal

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