Cleidocranial Dysplasia: A Case Report

Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease. CCD is caused by mutation in the gene on 6p21 encoding transcription factor CBFA1, i.e. runt−related transcription factor 2(RUNX2). The disease is characterized by a persistently open anterior fontanelle and skull sutures,...

Descripción completa

Detalles Bibliográficos
Autores principales: Karagüzel, Gülay, Aktürk, Filiz Azar, Okur, Emelgül, Gümele, Halit Reşit, Gedik, Yusuf, Ökten, Ayşenur
Formato: Texto
Lenguaje:English
Publicado: Galenos Publishing 2010
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005677/
https://www.ncbi.nlm.nih.gov/pubmed/21274329
http://dx.doi.org/10.4274/jcrpe.v2i3.134

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005677/
https://www.ncbi.nlm.nih.gov/pubmed/21274329
http://dx.doi.org/10.4274/jcrpe.v2i3.134

Ejemplares similares