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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3551519/ https://ncbi.nlm.nih.gov/pubmed/23393627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2156-7514.104303 |
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