Oral and Dental Changes of Dyskeratosis Congenita: A Case Report with Literature Review

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dc.contributor.authorSerindere, Gozde
dc.date.accessioned2024-09-18T20:16:35Z
dc.date.available2024-09-18T20:16:35Z
dc.date.issued2018
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractDyskeratosis congenita (DC) is an uncommon disease characterized by nail dystrophy, cutaneous hyperpigmentation, leukoplakia, pancytopenia, and malignant transformation. There can be some oral and dental changes such as oral leukoplakia, increase in tooth decay, hypodontia, thinning of enamel layer, aggressive periodontitis, intraoral brown pigmentation, missing tooth, taurodontism, and blunted roots. Most of cases belong to dermatology or pediatrics department. There are few reports about dentistry. The aim of this report is to lay emphasis on this fatal syndrome among dentists about the multisystem findings and oro-dental changes. Thus, this information may aid dentists in early diagnosis. A case of 21-year-old male diagnosed with DC is reported.en_US
dc.identifier.doi10.1177/2320206818789761
dc.identifier.endpage23en_US
dc.identifier.issn2320-2068
dc.identifier.issn2320-2076
dc.identifier.issue1-2en_US
dc.identifier.scopus2-s2.0-85086480894en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage20en_US
dc.identifier.urihttps://doi.org/10.1177/2320206818789761
dc.identifier.urihttps://hdl.handle.net/20.500.12483/9616
dc.identifier.volume9en_US
dc.identifier.wosWOS:000489324700005en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherSage Publications India Pvt Ltden_US
dc.relation.ispartofJournal of Advanced Oral Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDyskeratosis congenitaen_US
dc.subjectoral findingsen_US
dc.subjectdental treatmenten_US
dc.titleOral and Dental Changes of Dyskeratosis Congenita: A Case Report with Literature Reviewen_US
dc.typeReview Articleen_US

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