File:Cleidocranial dysplasia 01.jpg: Difference between revisions
(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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==Cleidocranial Dysplasia== | |||
Radiological findings for the patient. 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 | |||
===Reference=== | |||
<pubmed>28173761</pubmed> | |||
doi: 10.1186/s12881-017-0375-x. | |||
====Copyright==== | |||
© Wen’an Xu, Qiuyue Chen, Cuixian Liu, Jiajing Chen, Fu Xiong, Buling Wu. 2017 | |||
12881_2017_375_Fig1_HTML.jpg | 12881_2017_375_Fig1_HTML.jpg | ||
{{Footerf}} | |||
[[Category:Abnormal Development]][[Category:Bone]][[Category:Computed Tomography]][[Category:X-ray]] | |||
Revision as of 14:21, 13 February 2017
Cleidocranial Dysplasia
Radiological findings for the patient. 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
Reference
<pubmed>28173761</pubmed>
doi: 10.1186/s12881-017-0375-x.
Copyright
© Wen’an Xu, Qiuyue Chen, Cuixian Liu, Jiajing Chen, Fu Xiong, Buling Wu. 2017
12881_2017_375_Fig1_HTML.jpg
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
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| current | 14:18, 13 February 2017 |  | 518 × 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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