Show simple item record

dc.contributor.authorChopra, R
dc.contributor.authorMarwaha, M
dc.contributor.authorChaudhuri, P
dc.contributor.authorBansal, K
dc.contributor.authorChopra, S
dc.date.accessioned2020-12-18T04:23:01Z
dc.date.available2020-12-18T04:23:01Z
dc.date.issued2012
dc.identifier.citationChopra, R., Marwaha, M., Chaudhuri, P., Bansal, K. & Chopra, S. (2012). Hypodontia and delayed dentition as the primary manifestation of cleidocranial dysplasia presenting with a diagnostic dilemma.. Case Rep Dent, 2012, pp.262043-. https://doi.org/10.1155/2012/262043.
dc.identifier.issn2090-6447
dc.identifier.urihttp://hdl.handle.net/11343/256171
dc.description.abstractCleidocranial dysplasia is a rare autosomal disorder which manifests as partial or complete absence of clavicles, multiple supernumerary teeth, and delayed closure of fontanelle. Classical cases of cleidocranial dysplasia are easily diagnosed very early in the life. However, cases with partial manifestation of the syndrome and noncontributory family history are difficult to diagnose. Here, we report a case of 8.5-year-old girl child who presented with delayed tooth development (without any supernumerary teeth), anterior open fontanelle, and normal clavicles, thus resulting in a diagnostic dilemma.
dc.languageeng
dc.publisherHindawi Limited
dc.titleHypodontia and delayed dentition as the primary manifestation of cleidocranial dysplasia presenting with a diagnostic dilemma.
dc.typeJournal Article
dc.identifier.doi10.1155/2012/262043
melbourne.affiliation.departmentMelbourne Dental School
melbourne.source.titleCase Reports in Dentistry
melbourne.source.volume2012
melbourne.source.pages262043-
dc.rights.licenseCC BY
melbourne.elementsid1314210
melbourne.openaccess.pmchttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540686
melbourne.contributor.authorChopra, Radhika
dc.identifier.eissn2090-6455
melbourne.accessrightsOpen Access


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record