Results 41 to 50 of about 2,549 (207)
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 +2 more
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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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EDA Gene Mutations Underlie Non-syndromic Oligodontia [PDF]
, 2009 Recent studies have detected mutations in the EDA gene, previously identified as causing X-linked hypohidrotic ectodermal dysplasia (XLHED), in two families with X-linked non-syndromic hypodontia.
Wu, H. +7 more
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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 +4 more
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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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Analysis of AXIN2 gene mutations in a family with isolated oligodontia
口腔疾病防治, 2016 Objective To investigate the mutational characteristics of AXIN2 gene in a family affected by non⁃syn⁃ dromic oligodontia and to provide a molecular basis for studying the pathogenesis of oligodontia.
QIN Han +2 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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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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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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Progress in Orthodontics, 2018 Background Tooth agenesis can involve one or more congenitally missing teeth (CMT) and is the most common congenital dental anomalies in humans. Tooth agenesis and reduction of mesiodistal tooth width are reportedly associated, suggesting that the ...
Norihisa Higashihori +4 more
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