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dc.contributor.authorMohtasham, N
dc.contributor.authorNemati, S
dc.contributor.authorJamshidi, S
dc.contributor.authorHabibi, A
dc.contributor.authorJohari, M
dc.date.accessioned2018-08-26T09:31:28Z
dc.date.available2018-08-26T09:31:28Z
dc.date.issued2009
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57066
dc.description.abstractNevoid basal cell carcinoma syndrome, a rare autosomal dominant disorder, comprises a number of abnormalities such as multiple nevoid basal cell carcinomas, skeletal abnormalities and multiple odontogenic keratocysts. Considering the rarity of this syndrome, we present a 12-year-old boy affected by this syndrome. He had multiple okcs, calcification of falx cerebri, bifid ribs, frontal bossing and hypertelorism. Characteristic cutaneous manifestation (nevoid basal cell carcinoma) was not present in this patient. The jaw cysts were treated with marsupialization then enucleation. The dental clinician may be the first to encounter and identify this syndrome, when the multiple cystlike radiolucencies are discovered on panoramic view. © 2009 Mohtasham et al. licensee BioMed Central Ltd.
dc.language.isoEnglish
dc.relation.ispartofCases Journal
dc.subjectanamnesis
dc.subjectarticle
dc.subjectbasal cell nevus syndrome
dc.subjectcase report
dc.subjectchild
dc.subjectclinical feature
dc.subjectenucleation
dc.subjectfrontal bossing
dc.subjecthuman
dc.subjecthuman tissue
dc.subjecthypertelorism
dc.subjectjaw cyst
dc.subjectmale
dc.subjectodontogenic keratocyst
dc.subjectpanoramic radiography
dc.subjectschool child
dc.subjectthorax radiography
dc.titleOdontogenic keratocysts in Nevoid basal cell carcinoma syndrome: A case report
dc.typeReview
dc.citation.volume2
dc.citation.issue12
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1186/1757-1626-2-9399


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