Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation

Background  Cleidocranial dysplasia (CCD, #MIM119600) is an autosomal-dominant skeletal dysplasia characterized by delayed closure of the cranial sutures, aplasia, or hypoplasia of the clavicles and dental abnormalities. These findings were accompanied by mobile and drooping shoulders, frontal and p...

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Detalles Bibliográficos
Autores principales: Kalayci Yigin, Aysel, Duz, Mehmet Bugrahan, Seven, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837417/
https://www.ncbi.nlm.nih.gov/pubmed/35169780
http://dx.doi.org/10.1055/s-0041-1736482

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837417/
https://www.ncbi.nlm.nih.gov/pubmed/35169780
http://dx.doi.org/10.1055/s-0041-1736482

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