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Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations
Cleidocranial dysplasia (CCD) is a skeletal disorder affecting cranial sutures, teeth, and clavicles, and is associated with the RUNX2 mutations. Although numerous patients have been described, a direct genotype–phenotype correlation for RUNX2 has been difficult to establish. Further cases must be s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculdade De Odontologia De Bauru - USP
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239300/ https://www.ncbi.nlm.nih.gov/pubmed/35674542 http://dx.doi.org/10.1590/1678-7757-2022-0028 |