Results 51 to 60 of about 1,704 (199)

Is there any relationship between hypodontia and hyperdontia with taurodontism, microdontia and macrodontia? A retrospective study [PDF]

, 2020
Background: Hypodontia and hyperdontia may occur with other dental anomalies such as microdontia, taurodontism, talon cusp, macrodontia and germination.
KARGÜL, BETÜL
core   +1 more source

Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia

Clinical Genetics, Volume 110, Issue 1, Page 3-14, July 2026.
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise, Benkirane‐Jessel Nadia, Anton Nicolas, Vandamme Thierry, Clauss François, Conzatti Guillaume   +5 more
wiley   +1 more source

Endodontic Treatment of a Taurodontism Tooth: Report of a Case [PDF]

, 2008
Taurodontism is a rare dental anomaly in which the involved tooth has an enlarged and elongated body and pulp chamber with apical displacement of the pulpal floor.
MirMotalebi, Farshid, Nazari, Shahrzad
core   +1 more source

ORTHODONTIC PROBLEMS IN PATIENTS WITH HYPODONTIA AND TAURODONTISM OF PERMANENT MOLARS [PDF]

Journal of IMAB, 2011
Taurodontism is a morphological abnormality of the tooth shape with the following characteristic features: vertically enlarged pulp chamber, apical displacement of the bifurcation and trifurcation, shortened roots and no constriction at the level of the ...
Miroslava Yordanova, Svetlana Yordanova, G. Tomov   +2 more
doaj   +1 more source

Lived Experiences of Tooth Hypersensitivity in Children With Molar Incisor Hypomineralisation

International Journal of Paediatric Dentistry, Volume 36, Issue 4, Page 605-616, July 2026.
ABSTRACT Background Children with molar incisor hypomineralisation (MIH) can suffer from intense tooth hypersensitivity (TH), which may adversely affect various aspects of their emotional, social, and functional wellbeing. As TH diagnostic tools are primarily adapted from adult research, there is a clear need for a deeper understanding of MIH‐TH from a
Joana Monteiro, Fiona Gilchrist, Helen Rodd   +2 more
wiley   +1 more source

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

Journal of Clinical Periodontology, Volume 53, Issue 7, Page 1068-1099, July 2026.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple, Sotiria Gizani, Mariano Sanz, Dominique Declerck, Phoebus Madianos, Valerie Clerehugh, Monique Danser, Esti Davidovich, Janet Davies, Nikos Donos, Elisabeth Dursun, Elena Figuero, Filippo Graziani, Mervi Gursoy, Soren Jepsen, Clara Joseph, Moritz Kebschull, Norbert Kraemer, Tina Lambrinaki, Rodrigo López, David J. Manton, Joerg Meyle, Ana Molina, Lior Shapira, Cheryl Somani, Georgios Tsilingaridis, Svante Twetman, Nicola West, Biniyam Wondimu, Ferranti Wong, David Herrera   +30 more
wiley   +1 more source

Nonsurgical Endodontic Management of Oehler's Type II Dens Invaginatus Using a Combined High‐ and Low‐Viscosity Calcium Silicate‐Based Obturation Approach: A Case Report

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Dens invaginatus (DI) is a developmental anomaly characterized by the invagination of enamel and dentin into the pulp space, predisposing affected teeth to pulpal and periapical pathologies. The complex and irregular canal anatomy often complicates endodontic management.
Chloé Laporte, Davide Mancino, Maryline Minoux   +2 more
wiley   +1 more source

Klinefelter’s syndrome and taurodontism

Archivio Italiano di Urologia e Andrologia, 2019
Objective: Taurodontism is a dental anomaly characterized by an enlarged pulp chamber and apycal displacement of the pulpar floor. The prevalence of taurodontism in normal population is controversial. It has been reported that taurodontism is frequently observed in Klinefelter’s patients.
Emilia, Giambersio, Vincenzo, Barile, Antonio Marcello, Giambersio   +2 more
openaire   +3 more sources

Genotypes and Phenotypes of Patients With TSPEAR‐Related Disorder: Evidence of a Predominant Dental Phenotype

American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 790-799, April 2026.
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani, Lucia Tiberi, Annarita Giliberti, Elia Dirupo, Laila Zaroili, Francesco Brancati, Michela Brena, Stefano Caraffi, Chiara De Luca, Livia Garavelli, Anna Virginia Gulino, Milena Mariani, Marzia Pollazzon, Angelo Selicorni, Samuela Landini, Ilaria Sani, Rosangela Artuso, Angela Peron   +17 more
wiley   +1 more source

Association of taurodontism with hypodontia: a controlled study [PDF]

, 1989
Although taurodontism has been reported in many syndromes which also feature hypodontia, there have been no previous investigations on the prevalence of taurodontism in patients with hypodontia.
Seow, W. K., Lai, P. Y.
core