Results 1 to 10 of about 6,152 (269)
Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review [PDF]
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 +7 more
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Analyses of oligodontia phenotypes and genetic etiologies [PDF]
International Journal of Oral Science, 2021 Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of tooth agenesis. Many genes have been implicated in the etiology of tooth agenesis, which is highly variable in its clinical presentation.
Mengqi Zhou +14 more
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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 +5 more
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The oligodontia phenotype in a X-linked hypohidrotic ectodermal dysplasia patient with a novel EVC2 variant [PDF]
Heliyon, 2023 Objectives: To analyse the pathogenic genes in a patient with hypohidrotic ectodermal dysplasia (HED) and explore the relationship between pathogenic genes and the oligodontia phenotype.
Yi Wu +6 more
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Famlial nonsyndromic oligodontia
Contemporary Clinical Dentistry, 2012 Oligodontia is one of the most common developmental abnormalities in humans. The present case report highlights the features of oligodontia in a 12-year-old male patient which was managed successfully with multidisciplinary approach. Familial oligodontia
Punithavathy +4 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 +5 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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Oligodontia in Danish schoolchildren
Acta Odontologica Scandinavica, 2001 Oligodontia is a rare condition, and only limited data are available on its prevalence. The present paper is based on data from Danish schoolchildren. When these data are combined with comparable data on Danish schoolchildren published previously by the senior author, it is shown that oligodontia occurs in 0.16% of the children (95% confidence interval,
Steen Rølling, Sven Poulsen
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Zdravniški Vestnik, 2020 Background: Ectodermal dysplasia is a rare hereditary disease, characterized by defects in the development of two to five tissues derived from the embryonic ectoderm. As a part of the manifestation, oligodontia can occur.
Sonja Zarkovic Gjurin +3 more
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Isolated oligodontia in monozygotic twins [PDF]
European Journal of Dentistry, 2013 ABSTRACTThis case report defines a case of isolated oligodontia of 9 and 10 permanent teeth in 9-year-old monozygotic twin sisters and gives information about the possible genetic and environmental etiology, related dental anomalies and treatment options.
Koray Halıcıoğlu +4 more
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