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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,
Ricardo D Coletta +2 more
exaly +4 more sources
Nonsyandromic oligodontia: A rare case report
Medical Journal of Dr. D.Y. Patil University, 2015 Dental agenesis is the most common developmental anomaly in humans, which can be either in the form of anodontia, oligodontia, or hypodontia. Oligodontia can occur either as an isolated finding or as part of a syndrome.
Mayank Chaturvedi +3 more
doaj +2 more sources
Oligodontia and Facial Phenotype Associated with a Rare Syndrome
Case Reports in Dentistry, 2022 Introduction. Oligodontia is a dental abnormality in which the patient is missing teeth. It is a hereditary disorder characterized by agenesis of more than six primary or permanent teeth, excluding the wisdom teeth.
Fatima Ezzahra Zidane +1 more
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Analyses of oligodontia phenotypes and genetic etiologies
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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A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia. [PDF]
PLoS ONE, 2015 Oligodontia is defined as the congenital absence of six or more permanent teeth, excluding the third molars. Oligodontia may contribute to masticatory dysfunction, speech alteration, aesthetic problems and malocclusion.
Haochen Liu +3 more
doaj +2 more sources
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.
Yuko Iwamoto, Ryota Nomura, Yuria Asao
exaly +3 more sources
A Nonsyndromic Autosomal Dominant Oligodontia with A Novel Mutation of Pax9-A Clinical and Genetic Report [PDF]
Journal of Clinical and Diagnostic Research, 2015 Oligodontia is congenital absence of one or more teeth which has familial abnormality and attributable to various mutations or polymorphisms of genes often associated with malformative syndromes.
Umapathy Thimmegowda +4 more
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Novel PAX9 compound heterozygous variants in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9 variants [PDF]
Journal of Applied Oral Science, 2023 Studies have reported that >91.9% of non-syndromic tooth agenesis cases are caused by seven pathogenic genes. Objective To report novel heterozygous PAX9 variants in a Chinese family with non-syndromic oligodontia and summarize the reported genotype ...
Jiabao REN +11 more
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Clinical Case Reports, 2023 Key Clinical Message In this case report, we have highlighted the probability of coinciding multiple dental anomalies, such as SMMCI, taurodontism, and oligodontia.
Yasmin Sheikhhassani +2 more
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Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia [PDF]
Journal of Dental Research, Dental Clinics, Dental Prospects, 2022 Background. Hypodontia, or the absence of one or more teeth during tooth formation, is a highly prevalent dental anomaly. Nevertheless, the main causes are still unknown.
Shiva Safari +5 more
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