An Unusual Triplication of Supernumerary Teeth inPermanent Dentition: Report of a Rare Case
dc.contributor.author | Şener, Elif | |
dc.contributor.author | Özer, Nezaket Ezgi | |
dc.contributor.author | Şanlı, İlkay Aydoğdu | |
dc.date.accessioned | 2023-01-12T20:32:53Z | |
dc.date.available | 2023-01-12T20:32:53Z | |
dc.date.issued | 2021 | |
dc.department | N/A/Department | en_US |
dc.description.abstract | The word “synodontia or fusion” means union of two ormore teeth that affects both primary and permanent dentition. Althoughdouble teeth are relatively common with a reported prevalence rangingfrom 0.1% to 1.55%; the union of three teeth, named as triple teeth ortriplication, is rarely encountered in the primary dentition with a preva lence of 0.02%. Prevalence of triple teeth is well documented in pri mary dentition, but its occurrence in permanent dentition is a rarephenomenon. This article reports an unusual case of triplication of threesupernumerary teeth in permanent dentition associated with periapicalpathology in a 10-year-old male patient along with its clinical and ra diographic features illustrated using dental volumetric tomographyimaging. | en_US |
dc.identifier.doi | 10.5336/dentalsci.2020-80636 | |
dc.identifier.endpage | 723 | en_US |
dc.identifier.issn | 2146-8966 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 719 | en_US |
dc.identifier.trdizinid | 469024 | en_US |
dc.identifier.uri | https://doi.org/10.5336/dentalsci.2020-80636 | |
dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/469024 | |
dc.identifier.uri | https://hdl.handle.net/11454/81242 | |
dc.identifier.volume | 27 | en_US |
dc.indekslendigikaynak | TR-Dizin | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Türkiye Klinikleri Diş Hekimliği Bilimleri Dergisi | en_US |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | An Unusual Triplication of Supernumerary Teeth inPermanent Dentition: Report of a Rare Case | en_US |
dc.type | Article | en_US |