Broad Spectrum of Skeletal Malformation Complex in Patients with Cleidocranial Dysplasia Syndrome: Radiographic and Tomographic Study

PURPOSE: Cleidocranial dysplasia is an autosomal dominant disorder characterized by defective ossification of the intramembraneous ossification (primarily the clavicles, cranium, and pelvis), and it is caused by mutations in the RUNX2 gene that is responsible for osteoblast differentiation. Spine de...

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Detalles Bibliográficos
Autores principales: Al Kaissi, Ali, Ben Chehida, Farid, Kenis, Vladimir, Ganger, Rudolf, Radler, Christof, Hofstaetter, Jochen G., Klaushofer, Klaus, Grill, Franz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2013
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762605/
https://www.ncbi.nlm.nih.gov/pubmed/24023524
http://dx.doi.org/10.4137/CMAMD.S11933

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762605/
https://www.ncbi.nlm.nih.gov/pubmed/24023524
http://dx.doi.org/10.4137/CMAMD.S11933

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