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Treatment timing and multidisciplinary approach in Apert syndrome
Apert syndrome is a rare congenital disorder characterized by craniosynostosis, midface hypoplasia and symmetric syndactyly of hands and feet. Abnormalities associated with Apert syndrome include premature fusion of coronal sutures system (coronal sutures and less frequently lambdoid suture) resulti...
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| Publicado no: | Ann Stomatol (Roma) |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
CIC Edizioni Internationali
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4525098/ https://ncbi.nlm.nih.gov/pubmed/26330906 |
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