Results 41 to 50 of about 1,866 (155)

Prevalence of taurodontism in premolars

, 1986
Taurodontism does not involve molar teeth exclusively. To call attention to the occurrence of this phenomenon in premolars, 4,459 extracted mandibular and maxillary premolars were examined. Eleven showed evidence of taurodontism.
Faig Leite, H., Faig Leite, H. [UNESP], Niccoli, W. D. [UNESP], Simoes, S., Madeira, M. C. [UNESP], Simoes, S. [UNESP], Madeira, M. C., Niccoli, W. D.   +7 more
core   +1 more source

Taurodontism in 45,X Females

, 1990
Orthopantomograms of 87 45, X females, 61 first-degree female relatives of these females, and a population sample of 113 normal females and 44 normal males were examined for the occurrence of taurodontism in mandibular molars.
J. Varrela, L. Alvesalo, J. Mayhall
core   +1 more source

Taurodontism of deciduous molars: Report of two cases

SRM Journal of Research in Dental Sciences, 2014
Taurodontism, a disturbance of normal developmental of teeth where teeth lack normal constriction at the cervix with abnormally large rectangular tooth structure and pulp chambers.
Srikanth Hanasoge Srivathsa
doaj   +1 more source

Taurodontism in association with the cusp of carabelli: a report of 2 cases [PDF]

, 2011
Taurodontism is a malformation of multirooted teeth characterized by abnormally large pulp chamber and abnormally short roots. It is diagnosed by the use of radiographs.
Sote, EO, AO Ogunkola, EO Sote, Ogunkola, AO   +3 more
core   +1 more source

Dentofacial Characteristics in Patients With Epidermolysis Bullosa—A Cross‐Sectional Study

Clinical and Experimental Dental Research, Volume 12, Issue 5, October 2026.
ABSTRACT Objectives Epidermolysis bullosa (EB) is a rare genetic disease characterized by skin and mucosal fragility caused by pathogenic variants in structural protein genes. Malocclusions have been previously described in patients with EB, mainly in case reports, with no cohort studies characterizing dentofacial characteristics across all EB types ...
Sebastián Véliz, Susanne Krämer, Colomba Besa‐Witto, Pedro Diz‐Dios   +3 more
wiley   +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

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

High‐Power Surgical Laser for Treatment of Oral Manifestations of Mucopolysaccharidosis VI: A Case Report

Special Care in Dentistry, Volume 46, Issue 4, July/August 2026.
ABSTRACT Mucopolysaccharidosis type VI (MPS VI), a rare metabolic disorder, results from glycosaminoglycan accumulation in tissues, frequently leading to hyperplastic gingival alterations that necessitate comprehensive intervention. An 11‐year‐old male patient diagnosed with MPS VI required hospitalization due to complications associated with a ...
Regina Maria Raffaele, Mario Eduardo Baldo, Bianca Ribeiro Marques, Stefan Gabriel Gonçalves Martiniano, Gleyson Kleber do Amaral Silva, Rafael Ferreira   +5 more
wiley   +1 more source

Successful endodontic management of hypo, meso and hypertaurodontism: Two case reports

Contemporary Clinical Dentistry, 2012
Taurodontism is a morphoanatomical developmental anomaly rarely seen in teeth. Permanent mandibular molars are most commonly affected. Endodontic treatment of a taurodont tooth is challenging and requires special handling because of proximity and apical ...
Girish Kulkarni, K G Rajeev, P Ambalavanan, Krishnamurthy H Kidiyoor   +3 more
doaj   +1 more source