Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family

INTRODUCTION: Cleidocranial dysplasia (CCD) is an inherited disease caused by mutations in the RUNX2 gene on chromosome 6p21. This pathology, autosomal dominant or caused by a spontaneous genetic mutation, is present in one in one million individuals, with complete penetrance and widely variable exp...

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Detalles Bibliográficos
Autores principales: Impellizzeri, A., Midulla, G., Romeo, U., La Monaca, C., Barbato, E., Galluccio, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079435/
https://www.ncbi.nlm.nih.gov/pubmed/30123273
http://dx.doi.org/10.1155/2018/6591414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079435/
https://www.ncbi.nlm.nih.gov/pubmed/30123273
http://dx.doi.org/10.1155/2018/6591414

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