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Cleidocranial dysplasia presenting with retained deciduous teeth in a 15-year-old girl: a case report
INTRODUCTION: Cleidocranial dysplasia is a rare congenital defect of autosomal dominant inheritance caused by mutations in the Cbfa1 gene, also called Runx2, located on the short arm of chromosome 6. It primarily affects bones which undergo intramembranous ossification. This condition is of clinical...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3292823/ https://ncbi.nlm.nih.gov/pubmed/22260259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-6-25 |
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