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Related to Cleidocranial dysplasia: Gardner syndrome
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References in periodicals archive ?
Early craniofacial signs of cleidocranial dysplasia.
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype.
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.
Clinical spectrum of cleidocranial dysplasia in a family with twins.
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.
The therapeutic proposal for the alteration in the dentoalveolar complex, in the bearer of the cleidocranial dysplasia, involves the teeth restoration of the deciduous teeth when they present cavities, because their extraction does not necessarily induces the eruption of the permanent teeth (Shafer et al.
An interesting condition commonly associated with tooth eruption defects is cleidocranial dysplasia (CCD).
At Present, this congenital condition is known to be a generalized disorder of bone, and as such was renamed in 1978 cleidocranial dysplasia.