Results 21 to 30 of about 4,180 (225)

Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review

Dentistry Journal, 2023
The aim of this systematic review was to describe the clinical and genetic features of syndromes showing oligodontia as a sign. The review was performed according to the PRISMA 2020 checklist guidelines, and the search was conducted using PubMed, Scopus,
Natália Lopes Castilho, Kêmelly Karolliny Moreira Resende, Juliana Amorim dos Santos, Renato Assis Machado, Ricardo D. Coletta, Eliete Neves Silva Guerra, Ana Carolina Acevedo, Hercílio Martelli-Junior   +7 more
doaj   +1 more source

Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies [PDF]

, 2018
Objective: The aim of this study was the clinical and molecular characterization of a family segregating a trait consisting of a phenotype specifically involving the maxillary canines, including agenesis, impaction and ectopic eruption, characterized by ...
Barbato, Ersilia, Caputo, Viviana, Ciolfi, Andrea, Di Giorgio, Roberto, Genovesi, Maria Luce, Giovannetti, Agnese, Guarnieri, Rosanna, Magliozzi, Maria Rosa, Paolacci, Stefano, Pizzi, Simone, Pizzuti, Antonio, Tartaglia, Marco, Traversa, Alice   +12 more
core   +1 more source

Rare and Common Variants Conferring Risk of Tooth Agenesis [PDF]

, 2018
We present association results from a large genome-wide association study of tooth agenesis (TA) as well as selective TA, including 1,944 subjects with congenitally missing teeth, excluding third molars, and 338,554 controls, all of European ancestry. We
Alonso, I. (I.), Audolfsson, G. (G.), Bjornsdottir, G. (G.), Dhamo, B. (Brunilda), Feenstra, B. (Bjarke), Geller, F. (Frank), Gudbjartsson, D.F. (Daniel), Gudmundsson, L. (Larus), Gustafsson, O. (Omar), Howe, B.J. (B. J.), Ingason, A. (A.), Jonsson, L. (L.), Jonsson, R. (R.), Jonsson, T. (Thorvaldur), Leslie, E.J. (Elizabeth J.), Magnusson, T.E. (T. E.), Marazita, M.L. (Mary), Melbye, M. (Mads), Moreno Uribe, L.M. (L. M.), Nawaz, M.S. (M. S.), Nohr, C. (Christian), Oddsson, A. (A.), Olafsson, S. (S.), Ongkosuwito, E.M. (Edwin), Pinho, T. (T.), Rivadeneira, F. (F.), Santos, M. (M.), Stefansson, H. (Hreinn), Stefansson, K. (K.), Steinberg, S. (Stacy), Thordarson, A. (A.), Unnsteinsdottir, U. (U.), Vučić, S. (Strahinja), Walters, G.B. (Bragi), Wolvius, E.B. (Eppo), Zervas, M. (M.)   +35 more
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Nonsyndromic oligodontia in siblings: A rare case report

Journal of Pharmacy and Bioallied Sciences, 2014
A syndrome is a medical condition that is characterized by a particular group of signs and symptoms, involving several organ systems. Oligodontia is defined as the developmental absence of six teeth or more, excluding third molars.
Veerabadhran Mahesh Mathian, Murugesan Gawthaman, Ramachandran Karunakaran, Selvaraj Vinodh, Sundaram Manikandan, Alagappan Meenakshi Sundaram   +5 more
doaj   +1 more source

Interdisciplinary dental management of patient with oligodontia and maxillary hypoplasia: a case report

BMC Oral Health, 2022
Background The craniofacial developmental abnormality can significantly complicate the oral rehabilitation of patients with oligodontia. This case report describes an interdisciplinary approach that took 7 years to successfully treat a young patient with
Sharon Aronovich, Yuan-Lynn Hsieh, Richard Scott Conley, Bradley Stieper, Marilia Yatabe, Fei Liu   +5 more
doaj   +1 more source

Five-Year Follow-Up of a Child with Non-Syndromic Oligodontia from before the Primary Dentition Stage: A Case Report

Children, 2023
Background: Congenital absence of teeth is a major dental abnormality in pediatric dentistry and the absence of six or more teeth is defined as oligodontia.
Tatsuya Akitomo, Satoru Kusaka, Yuko Iwamoto, Momoko Usuda, Mariko Kametani, Yuria Asao, Masashi Nakano, Meiko Tachikake, Chieko Mitsuhata, Ryota Nomura   +9 more
doaj   +1 more source

New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742‐2A>G

Molecular Genetics & Genomic Medicine, 2023
Background Ectodermal dysplasias are inherited disorders, which are characterized by congenital defects in two or more ectodermal structures such as skin, sweat glands, hair, nails, teeth, and mucous membranes.
Vivian Reinhold, Stina Syrjänen, Minna Kankuri‐Tammilehto   +2 more
doaj   +1 more source

Frequency and characteristics of tooth agenesis among an orthodontic patient population [PDF]

, 2010
Purpose: The objectives of this study were to investigate the prevalence and characteristics of tooth agenesis and the associated skeletal morphology and arch widths in a group of Turkish patients seeking orthodontic treatment. Material and Methods: We
Celikoglu, Mevlut, Ceylan, Ismail, Kamak, Hasan, Kazanci, Fatih, Miloglu, Ozkan, Oztek, Ozkan   +5 more
core   +1 more source

Genetic basis of dental agenesis - molecular genetics patterning clinical dentistry [PDF]

, 2013
Tooth agenesis is one of the most common congenital malformations in humans. Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be associated with a syndrome (syndromic hypodontia), highlighting the heterogeneity of ...
Chhabra, Anuj, Chhabra, Nidhi, Goswami, Mridula   +2 more
core   +1 more source

Rehabilitation Considerations for Very Young Children with Severe Oligodontia due to Ectodermal Dysplasia: Report of Three Clinical Cases with a 2-Year Follow-Up

Case Reports in Dentistry, 2022
Introduction. Management of oligodontia can be complicated and requires multidiscipline care, involving a wide spectrum of interventions. The aim of this report is to describe the challenges of oral rehabilitation of three very young children with ...
Kyriaki Seremidi, Antigoni Markouli, Andreas Agouropoulos, Nick Polychronakis, Sotiria Gizani   +4 more
doaj   +1 more source