Familial Crouzon syndrome

Familial Crouzon syndrome

Crouzon syndrome is an autosomal dominant condition of the craniosynostotic syndromes without syndactyly and with various dentofacial anomalies. Craniosynostosis, maxillary hypoplasia, shallow orbits, ocular proptosis and hypertelorism are the characteristic features of Crouzon syndrome. This report...

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Bibliographic Details
Main Authors: Y Samatha, T Harsha Vardhan, A Ravi Kiran, A J Sai Sankar, B Ramakrishna
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-01-01
Series:Contemporary Clinical Dentistry
Subjects:
Craniosynostosis
Crouzon syndrome
dentofacial anomalies
Online Access:http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=4;spage=277;epage=280;aulast=Samatha

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http://www.contempclindent.org/article.asp?issn=0976-237X;year=2010;volume=1;issue=4;spage=277;epage=280;aulast=Samatha

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