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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Detalles Bibliográficos
Autores principales: C, Nagarathna, Shakuntala, Bethur Siddaiah, Mathew, Somy, Krishnamurthy, Navin Hadadi, Yumkham, Ratna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292823/
https://www.ncbi.nlm.nih.gov/pubmed/22260259
http://dx.doi.org/10.1186/1752-1947-6-25

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292823/
https://www.ncbi.nlm.nih.gov/pubmed/22260259
http://dx.doi.org/10.1186/1752-1947-6-25

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