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Complex dental anomalies in a belatedly diagnosed cleidocranial dysplasia patient
Cleidocranial dysplasia (CCD) is a rare congenital disorder, typically characterized by persistently open skull sutures, aplastic or hypoplastic clavicles, and supernumerary teeth. Mutations in the gene encoding the runt-related transcription factor 2 (RUNX2) protein are responsible for approximatel...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Korean Academy of Oral and Maxillofacial Radiology
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574057/ https://www.ncbi.nlm.nih.gov/pubmed/26389062 http://dx.doi.org/10.5624/isd.2015.45.3.187 |