Cleidocranial Dysplasia - A Rare Case Report

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dc.contributor.authorKosar, Shaminaen_US
dc.contributor.authorShah, Ajazen_US
dc.contributor.authorFarooq, Shahiden_US
dc.contributor.authorGul, Sumeraen_US
dc.contributor.authorBashir, Shabrozaen_US
dc.date.accessioned2019-12-06T09:24:05Z
dc.date.available2019-12-06T09:24:05Z
dc.date.issued2018-11
dc.description.abstractCleidocranial dysplasia is an autosomal dominant heritable disorder caused by mutation in the gene encoding transcription factor Core Binding Factor Subunit Alpha 1 (CBFA1) or Runt related transcription factor 2 (RUNX2). It is characterized by aplasia or hypoplasia of the clavicles, characteristic craniofacial malformations, and the presence of numerous supernumerary and unerupted teeth. A 37 year old male with cleidocranial dysplasia is described in this article with cyst associated with impacted teeth as the first presentation.en_US
dc.identifier.affiliationsPost Graduate, Department of Oral and Maxillofacial Surgery, Government Dental College, Srinagaren_US
dc.identifier.citationKosar Shamina, Shah Ajaz, Farooq Shahid, Gul Sumera, Bashir Shabroza. Cleidocranial Dysplasia - A Rare Case Report. Annals of International medical and Dental Research. 2018 Nov; 4(11): 5-7en_US
dc.identifier.issn2395-2822
dc.identifier.issn2395-2814
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/188402
dc.languageenen_US
dc.publisherSociety for Health Care & Research Developmenten_US
dc.relation.issuenumber11en_US
dc.relation.volume4en_US
dc.source.urihttps://doi.org/10.21276/aimdr.2018.4.6.DE2en_US
dc.titleCleidocranial Dysplasia - A Rare Case Reporten_US
dc.typeJournal Articleen_US
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