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      Meta-analysis and systematic review of factors biasing the observed prevalence of congenitally missing teeth in permanent dentition excluding third molars

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          Abstract

          No meta-analyses or systematic reviews have been conducted to evaluate numerous potential biasing factors contributing to the controversial results on congenitally missing teeth (CMT). We aimed to perform a rather comprehensive meta-analysis and systematic review on this subject. A thorough search was performed during September 2012 until April 2013 to find the available literature regarding CMT prevalence. Besides qualitatively discussing the literature, the meta-sample homogeneity, publication bias, and the effects of sample type, sample size, minimum and maximum ages of included subjects, gender imbalances, and scientific credit of the publishing journals on the reported CMT prevalence were statistically analyzed using Q-test, Egger regression, Spearman coefficient, Kruskal-Wallis, Welch t test (alpha = 0.05), and Mann-Whitney U test (α = 0.016, α = 0.007). A total of 111 reports were collected. Metadata were heterogeneous ( P = 0.000). There was not a significant publication bias (Egger Regression P = 0.073). Prevalence rates differed in different types of populations (Kruskal-Wallis P = 0.001). Studies on orthodontic patients might report slightly (about 1%) higher prevalence ( P = 0.009, corrected α = 0.016). Non-orthodontic dental patients showed a significant 2% decline [ P = 0.007 (Mann-Whitney U)]. Enrolling more males in researches might significantly reduce the observed prevalence (Spearman ρ = -0.407, P = 0.001). Studies with higher minimums of subjects' age showed always slightly less CMT prevalence. This reached about -1.6% around the ages 10 to 13 and was significant for ages 10 to 12 (Welch t test P < 0.05). There seems to be no limit over the maximum age (Welch t test P > 0.2). Studies' sample sizes were correlated negatively with CMT prevalence (ρ = -0.250, P = 0.009). It was not verified whether higher CMT rates have better chances of being published (ρ = 0.132, P = 0.177). CMT definition should be unified. Samples should be sex-balanced. Enrolling both orthodontic and dental patients in similar proportions might be preferable over sampling from each of those groups. Sampling from children over 12 years seems advantageous. Two or more observers should examine larger samples to reduce the false negative error tied with such samples.

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          A meta-analysis of the prevalence of dental agenesis of permanent teeth.

          To gain more insight into the prevalence of dental agenesis. Data from Caucasian populations in North America, Australia and Europe were included in a meta-analysis. For the prevalence of African American, Chinese and Arab groups only indications could be reported because of a limited number of studies. Agenesis differs by continent and gender: the prevalence for both sexes was higher in Europe (males 4.6%; females 6.3%) and Australia (males 5.5%; females 7.6%) than for North American Caucasians (males 3.2%; females 4.6%). In addition, the prevalence of dental agenesis in females was 1.37 times higher than in males. The mandibular second premolar was the most affected tooth, followed by the maxillary lateral incisor and the maxillary second premolar. The occurrence of dental agenesis was divided into three main groups: common (P2(i) > I2(s) > P2(s)), less common (I1(i) > I2(i) & P1(s) > C(s) & M2(i)) and rare (M2(s) & M1(s) > C(i) > M1(i) & I1(s)). Unilateral occurrence of dental agenesis is more common than bilateral occurrence. However, bilateral agenesis of maxillary lateral incisors is more common than unilateral agenesis. The overall prevalence of agenesis in the maxilla is comparable with that in the mandible, but a marked difference was found between both jaws regarding tooth type. Absence of one or two permanent teeth is found in 83% of the subjects with dental agenesis. A practical application of the results of the meta-analysis is the estimation of dental treatment need. Copyright Blackwell Munksgaard, 2004
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            Prevalence and distribution of dental anomalies in orthodontic patients.

            The purpose of this study was to determine the prevalence of developmental dental anomalies in the Turkish population. The study was based on the dental casts, intraoral photographs, and panoramic radiographs of 3043 Turkish children (1658 girls, 1385 boys) who had orthodontic treatment at the Department of Orthodontics at the University of Ankara between 1978 and 2003. These patients were examined for 8 developmental dental anomalies: fusion, gemination, microdontia, macrodontia, oligodontia, hypodontia, hyperdontia, and amelogenesis imperfecta. The percentages of these anomalies were assessed in the whole group, and the sexes were compared. It was found that 5.46% of the total group had at least 1 developmental dental anomaly. The distribution by sex was 70 boys (5.05%) and 96 girls (5.79%). Hypodontia is the most common developmental dental anomaly in the Turkish population, followed by microdontia.
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              Dental agenesis: genetic and clinical perspectives.

              Dental agenesis is the most common developmental anomaly in humans and is frequently associated with several other oral abnormalities. Whereas the incidence of missing teeth may vary considerably depending on dentition, gender, and demographic or geographic profiles, distinct patterns of agenesis have been detected in the permanent dentition. These frequently involve the last teeth of a class to develop (I2, P2, M3) suggesting a possible link with evolutionary trends. Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) involving one (80% of cases), a few (less than 10%) or many teeth (less than 1%), or can be associated with a systemic condition or syndrome (syndromic hypodontia), essentially reflecting the genetically and phenotypically heterogeneity of the condition. Based on our present knowledge of genes and transcription factors that are involved in tooth development, it is assumed that different phenotypic forms are caused by different genes involving different interacting molecular pathways, providing an explanation not only for the wide variety in agenesis patterns but also for associations of dental agenesis with other oral anomalies. At present, the list of genes involved in human non-syndromic hypodontia includes not only those encoding a signaling molecule (TGFA) and transcription factors (MSX1 and PAX9) that play critical roles during early craniofacial development, but also genes coding for a protein involved in canonical Wnt signaling (AXIN2), and a transmembrane receptor of fibroblast growth factors (FGFR1). Our objective was to review the current literature on the molecular mechanisms that are responsible for selective dental agenesis in humans and to present a detailed overview of syndromes with hypodontia and their causative genes. These new perspectives and future challenges in the field of identification of possible candidate genes involved in dental agenesis are discussed.
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                Author and article information

                Contributors
                vahid.rakhshan@gmail.com
                Journal
                Prog Orthod
                Prog Orthod
                Progress in Orthodontics
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                1723-7785
                2196-1042
                1 October 2013
                1 October 2013
                2013
                : 14
                : 33
                Affiliations
                Department of Dental Anatomy and Morphology, Dental Branch, Islamic Azad University, PO Box 19585-175, Tehran, Iran
                Article
                16
                10.1186/2196-1042-14-33
                4384895
                24325806
                526af7ec-5c13-4e59-820e-6e2e80ad0f1c
                © Rakhshan; licensee Springer. 2013

                This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 May 2013
                : 5 July 2013
                Categories
                Review
                Custom metadata
                © Italian Society of Orthodontics 2013

                congenitally missing teeth (hypodontia),permanent dentition,prevalence,sources of bias in the literature

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