Clinical implications of a diagnosis of taurodontism: A literature review.

dental pulp cavity endodontics genetic diseases tooth cervix

Journal

Advances in clinical and experimental medicine : official organ Wroclaw Medical University
ISSN: 1899-5276
Titre abrégé: Adv Clin Exp Med
Pays: Poland
ID NLM: 101138582

Informations de publication

Date de publication:
Dec 2022
Historique:
pubmed: 25 8 2022
medline: 22 12 2022
entrez: 24 8 2022
Statut: ppublish

Résumé

Taurodontism is a morphological anomaly involving multirooted teeth that is characterized by a vertical shift of the pulp chamber and shortening of the roots. The literature was analyzed to determine the impact of a diagnosis of taurodontism on dental treatment. A total of 85 full-text publications from the years 2005-2021 were analyzed and 20 publications were included in this research. The endodontic treatment of a taurodont tooth is challenging due to the apical displacement of the pulpal chamber floor and the incorrect configuration of the root canal system, or the presence of additional canals. In terms of prosthetics, the use of taurodont teeth as abutments is not recommended as they lack stability due to shorter roots. The extraction of taurodont teeth can be complicated due to an apical shift of the root furcation. In periodontology, taurodont teeth can have a better prognosis as there is less chance of furcation involvement. From an orthodontic point of view, it is important to note that taurodont teeth are not sufficiently embedded in the alveolus and have a greater tendency for root resorption. With regard to genetic diseases, it has been reported that this anomaly can exist as an isolated feature. However, the majority of authors agree that taurodontism is associated with conditions such as Down syndrome, Klinefelter syndrome, cleft lip and palate, hypodontia, amelogenesis imperfecta, and others. From a clinical standpoint, it is very important to diagnose taurodontism before treatment. A diagnosis of taurodontism can be important in the early diagnosis of malformations that commonly occur with this condition.

Identifiants

pubmed: 36000881
doi: 10.17219/acem/152120
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1385-1389

Auteurs

Janusz Pach (J)

Department of Comprehensive Dentistry, Medical University of Warsaw, Poland.

Piotr A Regulski (PA)

Department of Dental and Maxillofacial Radiology, Medical University of Warsaw, Poland.

Jacek Tomczyk (J)

Institute of Biological Sciences, Cardinal Stefan Wyszyński University, Warszawa, Poland.

Izabela Strużycka (I)

Department of Comprehensive Dentistry, Medical University of Warsaw, Poland.

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Classifications MeSH