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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Detalles Bibliográficos
Autores principales: Lu, Hui, Zeng, Binghui, Yu, Dongsheng, Jing, Xiangyi, Hu, Bin, Zhao, Wei, Wang, Yiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Oral and Maxillofacial Radiology 2015
Materias:
Case Report
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

Internet

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

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