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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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Detalles Bibliográficos
Autores principales:	Samatha, Y., Vardhan, T. Harsha, Kiran, A. Ravi, Sankar, A.J. Sai, Ramakrishna, B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications Pvt Ltd 2010
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220155/ https://www.ncbi.nlm.nih.gov/pubmed/22114439 http://dx.doi.org/10.4103/0976-237X.76402

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