cleidocranial dysostosis

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Related to Cleidocranial dysplasia: Gardner syndrome

cleidocranial dysostosis

[¦klī·dō¦krān·ē·əl ¦dis·ä′stō·səs]
(medicine)
A congenital defect in which there is deficient formation of bone in the skull and clavicle.
References in periodicals archive ?
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development.
A novel mutation in the C-terminal region of RUNX2/CBFA1 distal to the DNA-binding runt domain in a Japanese patient with cleidocranial dysplasia.
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.
RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
According to the clinical and radiographical findings, the diagnosis was a cleidocranial dysplasia.
In our case, the patient did not report the existence of direct ancestors or descendents who presented any clinical characteristic of cleidocranial dysplasia.
Although several bones in the body could present the cleidocranial dysplasia, the craniofacial characteristics consists of the main reason of the medical-odontological visits to the doctor.
Clinical and radiologic findings are suggestive of cleidocranial dysplasia.
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder with complete penetrance and variable expression.
Prenatal 3D Ultrasound Diagnostics in Cleidocranial Dysplasia.