Crouzon Syndrome: Clinico-Radiological Illustration of a Case

Crouzon syndrome, also called craniofacial dysostosis, is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder characterized by premature closure of cranial sutures, midfacial hypoplasia, and orbi...

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Detalles Bibliográficos
Autores principales: Mohan, Raviprakash Sasankoti, Vemanna, Naveen Shanker, Verma, Sankalp, Agarwal, Neha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551519/
https://www.ncbi.nlm.nih.gov/pubmed/23393627
http://dx.doi.org/10.4103/2156-7514.104303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551519/
https://www.ncbi.nlm.nih.gov/pubmed/23393627
http://dx.doi.org/10.4103/2156-7514.104303

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