File:Cleidocranial dysplasia 01.jpg

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Cleidocranial Dysplasia

Radiological findings for a patient with cleidocranial dysplasia.

a, b Cone-beam computed tomography results showing detailed dental abnormalities, including impacted supernumerary teeth, the retention of primary teeth, eruption failure of the permanent teeth, and impaired root development.

c, d A skull CT scan showed the presence of open fontanelles.

e Radiographs revealed hypoplastic or aplastic distal ends of clavicles and structural abnormalities occurring in the right shoulder peak joint.

Links: Musculoskeletal System - Abnormalities | Bone | Computed Tomography | X-ray



doi: 10.1186/s12881-017-0375-x.


© Wen’an Xu, Qiuyue Chen, Cuixian Liu, Jiajing Chen, Fu Xiong, Buling Wu. 2017

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Cite this page: Hill, M.A. (2024, April 25) Embryology Cleidocranial dysplasia 01.jpg. Retrieved from

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© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G

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current14:18, 13 February 2017Thumbnail for version as of 14:18, 13 February 2017518 × 700 (65 KB)Z8600021 (talk | contribs)A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia. Xu W, Chen Q, Liu C, Chen J, Xiong F, Wu B. BMC Med Genet. 2017 Feb 7;18(1):13. doi: 10.1186/s12881-017-0375-x. PMID 28173761 12881_2017_375_Fig1_HTML.jpg

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