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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Detalhes bibliográficos
Main Authors: Al Kaissi, Ali, Ben Chehida, Farid, Kenis, Vladimir, Ganger, Rudolf, Radler, Christof, Hofstaetter, Jochen G., Klaushofer, Klaus, Grill, Franz
Formato: Artigo
Idioma:Inglês
Publicado em: Libertas Academica 2013
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Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3762605/
https://ncbi.nlm.nih.gov/pubmed/24023524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/CMAMD.S11933
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