Otodental Syndrome

Authors:

M. Paglia
Department of Paediatric Dentistry, Istituto Stomatologico Italiano, Milano, Italy
M. Severino
Researcher Department of Medicine and Surgery University of Perugia, Perugia, Italy
R. Gatto
Ordinary Professor in Paediatric Dentistry, Department of Life, Health and Enviromental Science, Paediatric Dentistry, University of L’Aquila, L’Aquila, Italy
G. Giani
Private Practice in Busto Arsizio, Varese, Italy
S. Caruso
Department of Life, Health and Enviromental Science, Paediatric Dentistry, University of L’Aquila, L’Aquila Italy

DOI:

https://doi.org/10.23804/ejpd.2023.24.03.03

ABSTRACT

Background

Otodental syndrome is a rare autosomal dominant condition characterised by a dental phenotype known as globodontia often associated with high-frequency hearing loss. Globodontia occurs both in the decidous and permanent dentition and affects canine and molar teeth.

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Publication date:

September /2023

Issue:

Vol.24 – n.3/2023

Page:

247 – 249

Publisher:

Ariesdue

Topic:

Any other topic

Cite:

Harvard: M. Paglia, M. Severino, R. Gatto, G. Giani, S. Caruso (2023) "Otodental Syndrome", European Journal of Paediatric Dentistry, 24(3), pp247-249. doi: 10.23804/ejpd.2023.24.03.03

Vancouver: M. Paglia, M. Severino, R. Gatto, G. Giani, S. Caruso. Otodental Syndrome. European Journal of Paediatric Dentistry [Internet]. 2023Sep.4 [cited 2026May.25];24(3):247-249. Available from: https://www.ejpd.eu/abstract-pubmed/otodental-syndrome/

MLA: M. Paglia, M. Severino, R. Gatto, G. Giani, S. Caruso Otodental Syndrome. European Journal of Paediatric Dentistry. 2023;24(3):247-249

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.