Results 1 to 10 of about 294 (134)
Famlial nonsyndromic oligodontia
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
doaj +3 more sources
Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review
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 +3 more sources
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 +2 more
exaly +3 more sources
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia. [PDF]
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 +1 more source
Oligodontia and Facial Phenotype Associated with a Rare Syndrome
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
doaj +1 more source
A Nonsyndromic Autosomal Dominant Oligodontia with A Novel Mutation of Pax9-A Clinical and Genetic Report [PDF]
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
doaj +1 more source
Multidisciplinary Management of Oligodontia [PDF]
Agenesis of one or more teeth is one of the most common of human developmental anomalies. The term oligodontia refers to congenital absence of many but not all teeth whereas the term hypodontia implies the absence of only a few teeth. In the permanent dentition, hypodontia has a prevalence of 1.6% to 9.6%, excluding agenesis of the third molars ...
S M, Londhe, M, Viswambaran, P, Kumar
openaire +2 more sources
Novel PAX9 compound heterozygous variants in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9 variants [PDF]
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
doaj +1 more source
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
doaj +1 more source
Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia [PDF]
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
doaj +1 more source

