Genetic polymorphism in esr2 and risk of tooth agenesis
Rio de Janeiro Dental Journal (Revista Científica do CRO-RJ), 2019 Introduction: Tooth agenesis (TA) is the congenital absence of teeth. Several studies have proposed a strong genetic background for this condition. Aim: The present cross-sectional study aimed to evaluate whether genetic polymorphisms in the genes that code for estrogen receptors (ESR1 and ESR2) are associated with the presence of isolated TA in a ...
Marañón-Vásquez, Guido Artemio +7 more
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Orthodontic treatment need and prevalence of malocclusions in the Orthodontic Unit of "Sapienza - University of Rome" : a six - year clinical experience [PDF]
, 2019 AIM The objective of this epidemiological survey was to investigate the dental-skeletal features of subjects attending the Public Dental Service in U.O.C. (Orthodontic Department of “La Sapienza University of Rome) and compare them with the existing body
Giordano, Alessandra
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Availability Of Dental Anomaly Phenotype In Individuals With Familial Adenomatous Polyposis [PDF]
, 2014 Background: Mutations in the APC gene cause familial adenomatous polyposis (FAP), an autosomal dominant colorectal cancer predisposition associated with the development of hundreds to thousands of adenomatous colorectal polyps beginning in childhood or ...
Lewis, Andrea M
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Novel frameshift variant of WNT10A in a Japanese patient with hypodontia
Human Genome VariationCongenital tooth agenesis is caused by the impairment of crucial genes related to tooth development, such as Wnt signaling pathway genes. Here, we investigated the genetic causes of sporadic congenital tooth agenesis. Exome sequencing, followed by Sanger
Michiyo Ando +11 more
doaj +1 more source
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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Is Third-Molar Agenesis Related to the Incidence of Other Missing Teeth?
Turkish Journal of Orthodontics, 2014 Objective:The aim of this study was to investigate whether third-molar agenesis is related to agenesis of other missing teeth (incisor-premolar hypodontia [IPH]).Materials and Method:A sample of 94 Turkish patients with agenesis of upper lateral incisors
A. Burcu Altan, Ali Altuğ Bıçakçı
doaj +1 more source
Association of AXIN2 gene polymorphisms with nonsyndromic oligodontia in Turkish families
Dentistry 3000, 2016 Tooth agenesis is the most common developmental abnormality of the human dentition characterized by the congenital absence of one or more permanent teeth.
Nuriye Dinckan +3 more
doaj +1 more source
Patterns of tooth agenesis in individuals with Down syndrome
Special Care in DentistryAbstractAimsTooth agenesis (TA) is common in Down syndrome (DS). It is unknown whether this agenesis occurs in specific patterns, which is important regarding treatment planning and aetiological research. This study aimed to aggregate and analyze patterns of TA, excluding third molars, in individuals with DS using the tooth agenesis code (TAC).Methods ...
Sonja M. Kalf‐Scholte +3 more
openaire +3 more sources
Third molar agenesis among children and youths from three major races of Malaysians
Journal of Dental Sciences, 2012 Background/purpose: Third molar (M3) agenesis is linked to the evolution and growth of the human jaw, as it is the last tooth to develop in the human dentition.
Jacob John +5 more
doaj +1 more source