Apert syndrome and repercussions in Dental Medicine
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibroblast growthfactor receptor 2 (FGFR2), characterized by craniosynostosis, midface hypoplasia and syndactyly of the hands and feet. It has several oral manifestations, such as ogival palate, maxillary...
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| Formato: | article |
| Idioma: | eng |
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2020
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| Texto completo: | http://hdl.handle.net/10284/8582 |
| País: | Portugal |
| Oai: | oai:bdigital.ufp.pt:10284/8582 |