| Literature DB >> 19409168 |
Abstract
Crouzon syndrome is an autosomal dominant condition characterized by craniosynostosis with associated dentofacial anomalies. This report describes the different clinical features in two affected individuals of different families with particular reference to characteristic findings of this syndrome.Entities:
Mesh：
Year: 2009 PMID： 19409168 DOI： 05.2009/JCPSP.318320
Source DB: PubMed Journal: J Coll Physicians Surg Pak ISSN： 1022-386X Impact factor: 0.711