{"title":"Endodontic management of taurodontic mandibular second molar: A case report","authors":"Mohit Zarekar, Apurva Satpute, Mohini Zarekar","doi":"10.18231/j.ijohd.2023.054","DOIUrl":null,"url":null,"abstract":"Taurodontism is an infrequent dental anomaly that predominantly affects the molars and is commonly observed in conjunction with other anomalies or as a component of a syndrome. The phenomenon, previously regarded as a characteristic of early humans, is also observed in contemporary humans albeit with a lower incidence rate. This article presents a unique case study with a female patient who was 35 years old. The patient had taurodontism, a dental condition characterised by enlarged pulp chambers in the molars. Notably, this condition was not found to be connected with any further malformations or syndromes.","PeriodicalId":516738,"journal":{"name":"International Journal of Oral Health Dentistry","volume":"29 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Oral Health Dentistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18231/j.ijohd.2023.054","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Taurodontism is an infrequent dental anomaly that predominantly affects the molars and is commonly observed in conjunction with other anomalies or as a component of a syndrome. The phenomenon, previously regarded as a characteristic of early humans, is also observed in contemporary humans albeit with a lower incidence rate. This article presents a unique case study with a female patient who was 35 years old. The patient had taurodontism, a dental condition characterised by enlarged pulp chambers in the molars. Notably, this condition was not found to be connected with any further malformations or syndromes.