Crouzon's syndrome: A case report and review

Crouzon's syndrome: A case report and review

Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformations. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the 1st year of life. Herein, we report a case of this rare entity, a 12-year-old girl with...

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Bibliographic Details
Main Authors: Candice Jacinta Antao, Ajit D Dinkar, Manisha Khorate, Nigel R Figueiredo
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Journal of Oral Research and Review
Subjects:
Craniosynostosis
Crouzon's syndrome
maxillary hypoplasia
Online Access:http://www.jorr.org/article.asp?issn=2249-4987;year=2018;volume=10;issue=2;spage=87;epage=91;aulast=Antao

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