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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...
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| Gepubliceerd in: | Imaging Sci Dent |
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| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Korean Academy of Oral and Maxillofacial Radiology
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4574057/ https://ncbi.nlm.nih.gov/pubmed/26389062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5624/isd.2015.45.3.187 |
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