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Early orthodontic management of Crouzon Syndrome: a case report
Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. The disease is characteriz...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2009
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3454018/ https://ncbi.nlm.nih.gov/pubmed/23139476 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12663-009-0018-7 |
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