Results 51 to 60 of about 6,152 (269)
Estimation of dental age in children in a Turkish population with tooth agenesis
Contemporary Pediatric Dentistry, 2023 Aim: The aim of this study was to investigate tooth development according to chronological age in children with tooth agenesis and to determine whether the severity of tooth agenesis (hypodontia and oligodontia) has an effect on tooth development ...
Canan Bayraktar Nahir, Zuhal Kirzioglu
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Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review [PDF]
, 2014 Objectives: In the present study, it is described the phenotypical analysis and the mutational screening, for genes PAX9 and MSX1, of six families affected by severe forms of tooth agenesis associated with other dental anomalies and systemic entities ...
Arte, Sirpa +5 more
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Non-Syndromic Oligodontia of Primary and Permanent Dentition: 5 Year Follow Up- A Rare Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2013 Oligodontia designates the congenital absence of six or more permanent teeth, excluding the third molars. Oligodontia of primary and permanent dentition is a rare observance.
Joyson Moses +3 more
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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 +2 more
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Disturbances of dental development distinguish patients with oligodontia‐ectodermal dysplasia from isolated oligodontia [PDF]
Orthodontics & Craniofacial Research, 2017 Structured AbstractObjectiveTo investigate phenotypic differences in dental development between isolated oligodontia and oligodontia‐ectodermal dysplasia (ED).Setting and sample populationA total of 129 patients diagnosed with isolated oligodontia and 22 patients with oligodontia as part of ED were eligible.MethodsThe phenotype of dental development ...
B. Dhamo +5 more
openaire +5 more sources
Dental Management of Hypohydrotic Ectodermal Dysplasia: A Case Report [PDF]
Journal of Mashhad Dental School, 2020 Introduction: Ectodermal dysplasia is a genetic rare disease, consisting of a group of abnormalities which are the results of the abnormal development of two or more embryonic ectoderm derivatives, such as the skin, hair, nail, sweat gland, tooth, and ...
Koorosh teymoornezhad +2 more
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The association between Ponticulus Posticus and Dental Agenesis: a retrospective study [PDF]
, 2018 OBJECTIVE: Neural tube defects may increase the risk of an abnormal development of skull, vertebral column and teeth formation, including dental agenesis in non syndromic patients. The association between the presence of a congenital Dental Agenesis (DA)
Barbato, Ersilia +3 more
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Nonsyndromic Familial Oligodontia with Multiple Dens Invaginatus: A Case Report of an Unusual Case
Case Reports in Dentistry, 2013 Oligodontia is a rare dental anomaly with a prevalence of 0.3% in permanent teeth and much less frequency in the primary dentition. Familial oligodontia represents an absence of varying numbers of primary and/or secondary teeth as an isolated trait.
D. P. Vinuth +4 more
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IIUM Journal of Orofacial and Health Sciences, 2023 Oligodontia, a severe form of hypodontia characterized by the absence of multiple permanent teeth, presents considerable challenges in dental treatment.
Seng Boon Chu, Huay Shuan Ooi
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Progress in Orthodontics, 2018 Background The purpose of this cross-sectional study was to investigate the effects of congenitally missing teeth on craniofacial morphology and to characterize the features of maxillofacial morphology of oligodontia patients associated with individual ...
Yuki Takahashi +4 more
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