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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Hlavní autoři: Al Kaissi, Ali, Ben Chehida, Farid, Kenis, Vladimir, Ganger, Rudolf, Radler, Christof, Hofstaetter, Jochen G., Klaushofer, Klaus, Grill, Franz
Médium: Artigo
Jazyk:Inglês
Vydáno: Libertas Academica 2013
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Original Research
On-line přístup: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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