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. 2013 Oct 1;14:33. doi: 10.1186/2196-1042-14-33

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

Vahid Rakhshan 1,
PMCID: PMC4384895  PMID: 24325806

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.

Keywords: Congenitally missing teeth (hypodontia), Permanent dentition, Prevalence, Sources of bias in the literature

Review

Introduction

Congenital missing of teeth (CMT) or dental agenesis is a common dental abnormality, in which some dental buds fail to develop, leaving an empty space in the arch which causes numerous complications [119]. In most countries, out of every 10 to 20 individuals, at least one suffers from agenesis of at least one or two permanent teeth [1, 313, 16109]. It is of importance since not only it is very frequent (as the most common dental anomaly) [114], but also it needs difficult and expensive treatments [19, 105, 110, 111].

Considering the very high prevalence of CMT [114], its serious complications on esthetic and function [24, 1519, 56, 75, 77, 83, 86, 89],[97, 100, 105, 112117], and its challenging and costly multidisciplinary treatments [19, 105, 110, 111], studying it seems necessary for many fields. These involve public health, health insurance companies, anthropology, and of course multidisciplinary clinical practice (orthodontics, prosthodontics, pediatric dentistry, surgery, and general dentistry) [40, 105, 111, 117, 118].

The results pertaining to CMT are quite controversial. Although ethnicity accounts for a part of the debate [117] (V Rakhshan, unpublished work), a major source of dispute is the existence of different biasing factors in different reports. For example, enrolling younger subjects might increase the chance of encountering 'delayed’ tooth eruptions and mistakenly counting the empty spaces as CMT [18, 117]. Additionally, it is possible that researchers might tend to report the lower CMT prevalence in larger samples and vice versa [18, 117]. These and other biasing factors should be determined and avoided. Nevertheless, only the aforementioned two examples are meta-analyzed before, and in a small pool of 33 studies [117]. That meta-analysis confirmed the role of sample size but did not find any differences between studies with minimum ages of subjects older or younger than 7 years. They did not evaluate any other minimum ages or address the potential lack of test power due to their small sample. No other biasing factors have been analyzed thus far.

Moreover, recent studies are limited to carry out the sampling almost only from orthodontic and dental patients. This is possibly due to ethical concerns tied to X-ray exposure without any treatment need [18, 116]. Such samples are assumed to result in overestimation of CMT. However, it is not known whether this assumption is correct [86]. Besides, many studies do not sample an equal number of males and females. Females might somehow show higher CMT prevalence [10, 11, 17, 35, 36, 50, 82, 83],[91, 100, 117, 119] (V Rakhshan, unpublished work). Therefore, a question is whether enrolling more females can noticeably bias the CMT result (and if so, to which extent). Another possibility is that older patients might not remember their history of extraction, and therefore some extracted teeth might be considered as missing. Knowledge of the effects of these factors is of importance. However, no meta-analyses, systematic reviews, or even narrative reviews have explored these. The literature consists only of two rather narrow-scoped, small-sampled meta-analyses and two partially narrative literature reviews on CMT [115, 117, 120]. Hence, the aim of this study was to address the potential sources of bias of CMT prevalence, using more comprehensive search strategies and a larger sample.

Materials and methods

During September 2012 until April 2013, the author extensively searched for the keywords 'congenital missing of teeth’, 'CMT’, 'hypodontia’, 'oligodontia’, 'anodontia’, 'agenesis’, and 'prevalence’ [117], and combination of these words as well as their synonyms (for example, replacing 'missing’ with 'absence’, 'absent’, etc.; Table 1). Three Internet search engines [Pubmed, Thomson Reuters ISI Web of Science (WoS), and Google Scholar] were used by the author to search for relevant scientific articles (V Rakhshan, unpublished work).

Table 1.

Number of search results

Keyword Pubmed Web of Science Google Scholar Total
Variations of 'congenitally missing teetha 399 95 3,133 3,627
Hypodontia or anodontia or oligodontia 3,345 940 12,300 16,585
'Dental aplasia’ or 'dental agenesis’ or ’tooth aplasia’ or 'tooth agenesis’ 353 398 3,300 4,051
Congenitally missing teetha and prevalence 102 27 1,630 1,759
(Hypodontia or anodontia or oligodontia) and prevalence 490 170 3,560 4,220
(Dental aplasia or dental agenesis or tooth aplasia or tooth agenesis) and prevalence 100 106 1,560 1,766
Total 4,789 1,736 25,483 32,008

aIncluding the search results for congenital missing of teeth, congenital absence of teeth, and congenitally absent teeth.

Reports dealing with patients suffering from craniofacial syndromes or developmental disorders were excluded. Those including only primary dentition were as well excluded. The reports taking the rates of third molar missing cases (without presenting any information to filter third molars out) were excluded (V Rakhshan, unpublished work).

The inclusion criteria were as follows:

  • The presence of an English abstract or an abstract readable by the author; or when other studies cited local papers and provided useful information from earlier non-English papers on CMT in permanent dentition excluding third molars. The articles cited within the full texts were used after making sure that they meet the inclusion criteria.

  • The sample was representative of the underlying general population.

  • Diagnosis of dental agenesis was based on a radiographic examination (if not stated otherwise in them or in the citing articles).

  • Agenesis of third molars was excluded [117].

  • Data pertaining to at least one of the biasing factors of interest alongside CMT prevalence were present (V Rakhshan, unpublished work).

Not all the studies contained all the information simultaneously. As far as at least the prevalence and one biasing factor were reported by a study, it was used in this summary.

The texts of all the available full articles and the abstracts were read carefully by the author. Whenever the necessary data were available (regardless of analyses performed by articles' authors), all the percentages were recalculated. Raw data of one of them were inconsistent, as the two tables presenting the raw data did not match completely [88]. Every available English full text on CMT excluding third molars was read for at least twice. If there was a full text in another language, collecting any useful data piece was tried by means of translators or by digging for the presented numbers or English figure legends, etc. within the article. Some of those articles referred to other studies or reported briefly the previous studies. After making sure that those previous studies do not include third molars (or if they do, it is possible for us to filter or recalculate only information regarding hypodontia excluding third molars), they were included in this summary. Whenever it is possible to recover the raw data from the information, the percentages presented were recalculated and at many points fixed before reporting. Also, many studies had not reported some of the key elements. If possible, their raw data were carefully recovered from the combination of their text, graphs, and tables (V Rakhshan, unpublished work).

Statistical analysis

The reported prevalence rates in epidemiological studies were compared with those of orthodontic or dental patients, using a Kruskal-Wallis test and a Mann-Whitney U test. The level of significance was adjusted for the Mann-Whitney U test to 0.016, using the Bonferroni correction method for multiple comparisons. The association of publication year with reported CMT percentages was assessed in the literature and in the literature on Caucasians only, using a Spearman correlation coefficient. Also, the correlation between CMT prevalence and the ratio of enrolled male and female subjects in different studies was assessed using a Spearman coefficient. The Spearman coefficient was also used to analyze the potential association of sample size and CMT prevalence. Additionally, the scientific credit of each article was determined by checking its abstraction in Pubmed and Web of Science databases or both (the score 0 for none, 1 for each, and 2 for both); the correlation between the CMT and scores of the articles was evaluated using the Spearman coefficient. The potentially biasing role of minimum and maximum ages of enrolled subjects in different studies was assessed using the Spearman correlation coefficient. We tried to find also any cutoff age after which a significant decrease in CMT could be possibly observed. This was performed by comparing studies with minimum ages less or greater than each cutoff using a Welch t test. The same test was used in the same fashion to possibly find a cutoff point for the maximum age.

Results

About 24,000 studies were initially found via various search engines which this reduced to about 8,000 more relevant results (Table 1) and then to about 2,500 studies without counting the repetitions in different search engines. Searching was updated during the study period to find newly emerged articles, and one new relevant study was published in March 2013. The excluded studies were the duplicated ones (in different search websites), those with no reference to the exclusion of third molars or syndromes, or those pertaining to other aspects of CMT without presenting at least CMT prevalence in permanent dentition and at least one biasing factor. If at least they had graphs or tables from which the CMT prevalence could be recovered and/or the data allowed us to exclude third molars and syndromes, the prevalence would be calculated manually. All the procedures were done for at least twice by one examiner (and for some articles, more than two times). Finally, 111 reports were included in this review (Table 2) [1, 313, 16109, 121] (V Rakhshan, unpublished work).

Table 2.

The reported frequencies on missing of all permanent teeth except the third molars

Year Country Type Prevalence Year Country Type Prevalence Year Country Type Prevalence
1936 Switzerland SC 3.4 1974 Canada SC 7.4 2001 Kenya OP 6.3
1939 - - 2.3 1976 Sweden SC 7.4 2001 Hungary OP 15.7
1943 USA 2.8 1977 Iceland SC 7.9 2001 Korea SC 8.0
1949 Japan St 15.9 1977 Sweden SC 7.4 2002 Norway PuDP 4.5
1951 Japan SC 5.6 1977 Japan - 8.6 2002 Iraq OP 8.9
1954 Japan SC 8.7 1979 USA SC 7.4 2002 S Arabia PeDP 3.6
1955 Japan DS 1.4 1980 Denmark SC 7.8 2003 Mexico OP 2.7
1956 Sweden SC 6.1 1980 Denmark SC 7.7 2005 Slovenia OP 11.3
1956 USA DP 3.7 1987 Hong-Kong SC 6.9 2006 Japan OP 10.1
1959 Sweden - 7.4 1988 Japan OP 9.9 2006 Jordan DP 5.5
1961 USA DP 5.2 1989 Malaysia SC 2.8 2006 Hungary OP/PeDP 14.7
1963 Norway SC 4.5 1989 Australia DP 6.4 2007 Turkey OP 7.5
1963 Austria SC 9.6 1989 Italy DP 5.2 2007 Turkey OP 2.8
1963 Japan SC 6.6 1989 USA PeDP 7.8 2008 Italy OP 9.5
1964 USA DP 5.1 1989 S Arabia DP 2.2 2008 Japan PeDP 9.8
1965 Israel SC 0.3 1989 Ireland - 11.7 2008 Brazil PeDP 4.8
1966 UK OP 4.3 1989 Czechoslovakia - 4.1 2008 Korea OP 11.2
1963 Canada DP 4.2 1990 S Arabia SC 4.0 2009 Spain OP 6.5
1966 USA 6.5 1990 Japan PeDP 16.2 2009 Turkey DP 73.4
1967 USA SC 3.8 1990 Thailand OP 8.6 2010 Pakistan OP 9.0
1967 USA SC 4.1 1990 Australia DF 6.3 2010 India DP 0.1
1968 Australia SC 5.9 1990 Ireland OP 11.3 2010 Iran DP 9.0
1968 Denmark SC 6.1 1990 Yugoslavia-Istria OP 6.3 2010 Turkey OP 4.6
1970 USA St 3.5 1990 Yugoslavia-Slavonia OP 2.3 2010 Spain PHS 7.3
1970 USA St 3.6 1991 Italy DF 3.6 2010 Iran OP 9.1
1971 Finland SC 8.0 1992 Japan OP 10.9 2010 S Arabia OP 7.0
1971 - - 5.5 1992 - OP 5.3 2010 Turkey DP 1.5
1971 Sweden SC 6.3 1993 Norway SC 6.5 2011 Korea OP 11.3
1972 Japan SC 9.2 1994 Germany OP 8.1 2011 Korea DP 5.7
1972 Japan OP 11.0 1995 Japan PeDP 2.8 2011 India DP 4.5
1973 Israel - 4.6 1996 Mexico OP 6.3 2011 Germany OP 13.1
1973 Denmark 8.2 1997 Iceland SC 4.3 2012 Iran OP 9.0
1973 Norway SC 10.1 1997 Estonia SC 14.0 2012 India SC 0.3
1973 Sweden SC 6.1 1998 China - 7.3 2012 Turkey PeDP 6.2
1974 UK SC 4.4 1999 S Arabia DP 4.2 2012 Portugal DP 6.1
1974 Switzerland SC 7.7 1999 Brazil OP 6.3 2012 S Arabia DP 4.7
1974 Norway SC 6.8 1999 Japan OP 9.4 2012 Iran OP/DP 10.9

DS, dental student; OP, orthodontic patients; SC, schoolchildren; PuDP, public dental patients; PeDP, pediatric dental patients; DF, defense force recruits; PHS, attendees to the primary health services; DP, dental patients other than orthodontic patients.

A single study was published in two different journals (one indexed in Pubmed and the other not indexed in any accredited databases), in the same year, without showing any noticeable difference in the content (thus both were considered as a single report) [95, 122]. The sample of Gabris et al. [78] seemed to be used as a subsample in their other study [85], although it is not known for sure as they did not suggest it. Syndrome cases were removed by the author from the study of Galluccio and Pilotto [87]. Cleft palate cases were excluded by the author, and the prevalence was recalculated for the study of Behr et al. [105]; however, four patients among their remaining cases were syndromic. From the study of Ghaznawi et al. [74], third molars were excluded by the author. Osuji et al. [81] reported only the missing of teeth anterior to molars. The sample of Sheikhi et al. [121] and Gabris et al. [85] were composed of both dental and orthodontic patients but the ratio of each was not known. A research had reported the maximum age as both 25 and 53 in different parts of the article [121]. Their maximum age was not used in analyses.

Homogeneity of metadata

Data were heterogeneous (Q = 7287.8, I2 = 98.5, P = 0.000) meaning that besides the sampling error due to the differences in the samples, other factors accounted for the different results as well.

The biasing role of sample types

Studies on orthodontic patients might report prevalence rates about 1% greater, while those of dental patients might report prevalence rates about 2% smaller than epidemiological studies (Figure 1). The Kruskal-Wallis test showed that the difference between reports on epidemiological samples versus orthodontic and dental patients is significant (P = 0.000). The Mann-Whitney U test showed that the pairwise comparisons were as well significant between epidemiological samples with dental patients (P = 0.007) and orthodontic patients (P = 0.009), and also between orthodontic and non-orthodontic dental patients (P = 0.000, corrected α = 0.016).

Figure 1.

Figure 1

Box plots for different CMT prevalence rates in three population types. Taking into analysis 43 epidemiological studies, 32 studies of orthodontic patients, and 29 studies on dental patients. Pediatric dental patients are categorized as dental patients.

Compositions of samples in terms of sex balance

The Spearman coefficient showed a significant correlation between CMT prevalence and male/female ratios (calculated by dividing the number of male subjects by females subjects) (n = 62, ρ = -0.407, P = 0.001).

Minimum age of included subjects

The minimum age was not significantly correlated with CMT (n = 79, ρ = -0.131, P = 0.255, Figure 2). Each minimum age was used as a cutoff to examine whether at any specific minimum age, there is a possibility to see significant differences between the CMT reported by studies adopting subjects younger and older than that age (Table 3). The comparisons were done using an unpaired t test with Welch correction. An almost steady reduction was seen for most of the cutoffs, between studies adopting subjects with minimum ages less than each cutoff and those enrolling minimum ages over that cutoff. At the age of 10 (comparing <10 with ≥10), the CMT prevalence was significantly different between studies with minimum ages set at less than 10 and those at 10 or older (P = 0.018). This also happened at the age 11 (P = 0.028) and 12 (P = 0.033). The highest difference was observed at the age of 13, but it was only marginally significant (Table 3).

Figure 2.

Figure 2

Box plots illustrating CMT of studies with different minimum ages of subjects.

Table 3.

Results of Welch t test comparing studies' CMT results (%) according to various minimum ages

Cutoff age (year) <Cutoff ≥Cutoff
N Mean (%) N Mean (%) Difference P value
6 13 5.85 64 6.27 0.42 0.704
7 28 6.41 49 6.08 -0.33 0.687
8 37 6.39 40 6.02 -0.36 0.62
9 42 6.42 35 5.93 -0.49 0.49
10 50 6.77 27 5.14 -1.64 0.018
11 54 6.68 23 5.06 -1.63 0.028
12 57 6.64 20 4.94 -1.70 0.033
13 64 6.52 13 4.60 -1.92 0.074
14 66 6.39 11 5.05 -1.34 0.239
16 71 6.34 6 4.50 -1.84 0.011

N number of studies.

Maximum age of included subjects

The Spearman coefficient showed no significant correlation between the maximum ages and CMT prevalence (n = 73, ρ = -0.003, P = 0.978). Ages 15, 20, 25, 30, 35, 40, 45, and 50 were considered potential cutoffs. The comparison of the results of studies with maximum ages of patients less than or above these cutoff ages showed no significant differences. An outlier study with CMT = 71.38% was in the analysis. After removing the outlier, the rest were re-analyzed. Although the results were nonsignificant, at the cutoff maximum age of 45 years, the P value showed a peak from values >0.8 to 0.242, and the difference changed from about 0.5% to 2% but still nonsignificant (i.e., the studies enrolling older ages showed about 2% greater CMT rates).

Sample size as a biasing factor

The sample size was significantly and negatively correlated with CMT (n = 109, ρ = -0.250, P = 0.009).

Publication bias

By analyzing the potential asymmetry in the funnel plot (Figure 3), the Egger regression test pointed to a marginally significant publication bias (intercept = 2.81, SE = 1.55, 95% CI = -0.26 to 5.90, P = 0.073).

Figure 3.

Figure 3

A rather symmetrical funnel plot (with some outliers) of study precisions against effect sizes.

Correlation between scientific level of journals and the reported CMT prevalence

The one study published in two different journals was considered as Pubmed-indexed. The outlier study of Peker et al. [91] was excluded from the analysis. There was no significant link between the credit of the article and the CMT prevalence reported (n = 107, ρ = 0.132, P = 0.177). The same analysis was done for studies published after 1990, and the association was still nonsignificant (n = 54, ρ = 0.182, P = 0.188).

Discussion

The literature consists of so many studies on the prevalence of CMT in permanent dentition (excluding third molars) among different populations [1, 313, 16109, 114, 123125]. The results are extremely controversial, ranging from 0.1% to 16.2% and varying considerably in many countries. However, they mostly revolved around 7% [mean = 6.72 ± 3.28, n = 110 (excluding one unreliable outlier showing 74%)] [1, 313, 16109]. The different rates reported could be explained by the ethnic backgrounds [4, 18, 54, 100, 112, 117, 118] and variations in the samples with respect to sample sizes, types, and other biasing factors [2, 3, 18, 86, 117]. Another (unpublished) meta-analysis of this author shows that CMT may happen more in Yellow race and perhaps in Europeans, while it is less common in the west of Asia and America. Also this anomaly is not being increased in epidemiological samples through time, although inclusion of dental patients in recent studies is biasing this results (V Rakhshan, unpublished work). The variations are not only a reflection of ethnicity, but can occur due to biasing factors as well. Discerning the responsible sources of bias can benefit future studies.

Should studies be sex-balanced?

Samples not balanced in terms of gender can bias the result, as CMT is more likely to occur in females [10, 11, 17, 35, 36, 50, 82, 83],[91, 100, 117, 119] (V Rakhshan, unpublished work). Our statistical analysis confirmed the role of the male/female ratio in affecting the prevalence. This ratio was considerably different from 1.0 in many studies (Figure 4). Such designs should be avoided in the future.

Figure 4.

Figure 4

Frequency distribution of 63 ratios of enrolled male and female subjects. Frequency distribution (%) of 63 ratios of enrolled male and female subjects, excluding one study with a male/female ratio of 4.21 [16] and two studies on only males [61, 66]. The blue bar is indicative of gender-balanced samples. Ratios greater than 1 show a gender imbalance in favor of males, and those smaller than 1 denote more females.

Do minimum and maximum ages of included subjects matter?

Calcification of teeth usually completes until the age of 9 years. Sometimes calcification of premolars is delayed [18, 69, 74, 86]. The absence of a premolar in a radiograph cannot be certainly regarded as missing until this age, or the age of 10 years [117], particularly in boys [18, 77, 86, 98, 102]. Therefore, patients should be assessed in the third and fourth dental stages (DS), during which canines/premolars erupt and occlude with their antagonist teeth, respectively [102]. Inclusion of DS 1 and DS 2 (eruption and occlusion of incisors) and earlier stages should be avoided [102]. Some evidences clearly confirm the decrease of the observed CMT prevalence in a single population after 2 years (7-year old children compared to themselves at the age of 9) [18, 48, 86]. This can compromise studies which have enrolled subjects as young as 5 [100, 126] or 7 years old [4, 121]. It probably causes high prevalence of second mandibular premolar missing (and also general CMT) [3, 10, 17, 48, 117]. Second premolars can develop long after what it would be ordinarily expected, reducing the degree of certainty [3]. Therefore, some authors have recommended exclusion of children younger than 7 [3], 9 or 10 years old [18, 77, 86, 98, 117], or even under 16 [18]. Nevertheless, some authors refuted this by following a population of 7-year-old children evaluated first in 1976 until 1990 [4]. They found that only one out of 739 subjects showed late mineralization of teeth. They concluded that samples with minimum ages lower than 9 might as well lead to reliable results [4]. Also Varela et al. [75] assessed children under 10 years old with dental agenesis some years later and found no tooth germs in the place of previously found missing teeth [75].

Polder et al. [117] evaluated the prevalence reported in 33 studies stratified into those with older and younger than a minimum inclusion age of 7 years old. They did not find a significant difference (P = 0.42). The same happened in our study, when ages 6, 7, 8, and 9 were the cutoff ages. Nevertheless, we investigated more ages as cutoffs. The post-cutoff decrease reached the level of significance when it came to the ages 10, 11, and 12. Therefore, it seems that by enrolling people older than these ages, overestimation of CMT (due to false positive diagnosis of missing) is considerably reduced and these can be possibly considered of the best minimum ages. However, at older ages such as 16 as well, significant differences emerged, which imply that false positive diagnosis might occur even until 16. Since the number of subjects at a minimum age set by each study is not known, the mentioned minimum age does not necessarily reflect that a considerable part of a sample are at that minimum age or around it. This can blur the link between the stated minimum age and CMT. However, there was still a reduction (even if nonsignificant) for almost all the cutoff ages. It validates the claim that there might be a share of false positive in younger ages (which can be generalized at ages 10 to 12). It might be recommended to avoid the inclusion of subjects younger than 12 or 13, in order to make sure an empty space seen in the radiograph at that age is almost only a case of missing, not a delayed tooth bud development. Of course sampling from older ages (such as older than 16) is better [18], but this has a trade off with the ease of finding proper test subjects.

It was hypothesized that perhaps enrolling older subjects might increase the false positive error due to the addition of the extracted teeth into the sample. Two reasons are imaginable for the lack of significance. First, many studies enrolled only full sets of dentition (regardless of patients' age). Second, a few studies had high maximum ages.

Do orthodontic or other dental patients necessarily show 'greater’ missing rates?

It is suggested that children with CMT may be more prone to visit orthodontists compared to individuals without missing, which this can affect the findings [5, 17, 18, 37, 86, 125, 127]. However, Sisman et al. [86] showed that CMT prevalence is similar for orthodontic patients and epidemiological populations. On the other hand, our analyses showed that studies of orthodontic and other dental patients might have a slight but still statistically significant error (Figure 1). It was interesting that the prevalence rates reported by studies on dental patients (except orthodontic patients) were unexpectedly smaller than epidemiological samples. It seems that enrolling orthodontic patients should be accompanied with enrolling dental patients in similar ratios, in order to possibly offset or reduce their biasing roles at opposite directions. However, this needs further studies.

Do smaller studies report higher prevalence?

It might be plausible that when fewer research subjects are available, there might be a bias to catch more cases of interest. Also in larger studies, it is possible that exhausted researchers overlook some of existing cases. As well, small studies with low prevalence of dental agenesis might be less likely to be submitted or accepted for publication [117]. Therefore, smaller studies might show larger prevalence rates. Our findings confirmed that the sample size correlates negatively with the CMT. It is not easily known, however, whether the smaller prevalence rates are closer to reality or the greater ones, because there is no gold standard to estimate the sensitivity and specificity of these two and conduct receiver-operator curves. However, it can be recommended that sufficiently large samples (based on a priori power calculation) should be assessed by two or more observers. This way, the advantages of a larger sample remain while the odds of false negative errors reduce.

Do greater CMT prevalence rates have better chances of being published?

It was suggested that smaller samples with smaller CMT rates might have less chances to be published [117]. Our analysis could not verify this, although a marginally significant asymmetry was detected in the funnel plot. This lack of significant publication bias could be due to the rather more extensive literature search done in this study, which allowed many non-English and average articles to be pooled. Therefore, the author tried to assess whether such a trend exists. A higher chance of publication can increase the publication likelihood in acclaimed journals. So if better journals published higher CMT prevalence rates, the above assumption might be confirmed. Also since many studies published in the previous century were reported in accredited but not indexed journals, we repeated this analysis for studies published after 1990 (when the Pubmed and WoS databases were more popular in dental literature). Nevertheless, although the correlation increased slightly, it was still nonsignificant (in part due to the reduction in the new sample size). Therefore, we could not verify that if higher CMT prevalence rates have a greater chance of publication. It should be noted that although we tried to include local journals as well (if found by searching), there might be still many studies ruled out in this meta-sample due to the language bias.

Other potential limitations and sources of bias

A limiting obstacle is the difficulty to accurately distinguish the absent tooth from adjacent similar teeth [102]. This is noticeable especially in the case of mandibular incisors when there are three incisors [3, 18, 102], for which meticulous examination of dental casts can be helpful [89, 102]. It can be more difficult when the other teeth have moved, and also when the image of the vertebrae is superimposed on the anterior mandible [3].

Clinical examinations may cover merely 70% of actual cases of CMT, and radiographic examination is always necessary [3, 18, 93]. However, X-ray exposure for whatever purposes except treatment is unethical (even screening, since it is not effective [57]) [18, 116]. Besides, orthodontic materials are appropriate for diagnosing CMT [89]. Therefore, recent papers are enrolling only orthodontic or dental patients. Our analyses showed that orthodontic patients or dental patients might show about 1% to 2% error compared to epidemiological samples, but there seems to be no other choice. Some studies enrolled epidemiological populations but reduced the number of radiographs taken, by clinically examining the area at first and ordering X-ray exploration if in doubt. Nevertheless, this method might introduce sampling bias [117].

Why should definitions be unified?

Another issue can be the variation in definitions. Specific terminologies are used to describe the nature of tooth agenesis. In general, the term hypodontia is most commonly used to describe the phenomenon of CMT [83]. Many other terms to describe a reduction in the number of teeth appear in the literature: oligodontia, anodontia, aplasia of teeth, congenitally missing teeth, absence of teeth, lack of teeth, and agenesis of teeth [83]. Hypodontia, oligodontia, and anodontia differ in terms of the number of missing teeth. Nevertheless, there is no clear consensus over the threshold differentiating hypodontia from oligodontia [3, 100, 114]. The categories used for defining oligodontia is the absence of more than three [16, 113], more than four [5, 89], more than five [3, 15, 48, 79, 91, 96, 100, 102],[105, 114, 117, 118, 128], more than six teeth [82, 83, 98, 104, 114], and even more than ten teeth [69, 129], always excluding the third molars [3]. Some authors did not define their threshold [1].

In some studies, the problem was beyond using different definitions. They basically confused the terms. For example, some investigators reported CMT under the name hypodontia [4, 19, 75, 77, 89, 90, 94, 98],[102, 106]. A study reported hypodontia as CMT [109]. Some even reported oligodontia cases as a part of hypodontia (again implying that hypodontia was considered CMT) [98, 102]. A study considered hypodontia as people with missing cases less than six teeth but more than two [105]. Some studies did not give any clear clue as if they were referring to CMT by hypodontia or not [4, 75, 106, 130]. In some of them, there were certain vague (but not official) remarks implying that perhaps the CMT was the case [4, 75, 130]. All of the above-mentioned variations can account for the high heterogeneity observed in this meta-sample.

It might seem that the percentages reported by the erroneous definitions should be similar usually, as oligodontia has a low frequency. For example, two studies which mistook CMT with hypodontia, showed only one subject with more than six absent teeth [4] or even not more than six missing teeth [77]. Therefore, their CMT results [77] might be pointing to hypodontia as well. Besides, since the prevalence of missing of four or more teeth is scarce, changing the threshold of hypodontia definition from >3 teeth to >6 teeth might lead to slight changes only.

Nevertheless, in some populations, it can still account for some more vivid changes. About 10% to 25% of hypodontia cases are individuals with more than two teeth missing [46, 8, 10, 13, 17, 18, 27, 36],[40, 41, 46, 4850, 53, 54, 62, 76],[77, 79, 81, 86, 88, 89, 102, 106],[117, 125, 127]. About 5% of the population might have more than three missing teeth [89] or about 5.5% might have four and about 1.5% might have five absent teeth [86]. There can be about 6% and 5.4% prevalence of patients with four and five teeth missing, respectively in Japanese [3], about 7% prevalence for four missing teeth in Brazil [88], 7% prevalence of more than five missing teeth in Turkey [91], or 16% of more than five absent teeth in Germany [105]. Therefore, the unification of these terminologies as CMT instead of hypodontia etc., and using standardized templates to clearly define CMT and mild, moderate, and severe cases of CMT or hypodontia are necessary.

Conclusions

Limitations of previous reports make comparisons difficult and at some points impossible. A need for a standardized template is perceived to unify methodologies and also enable researchers to assess this issue with the most possible details.

Future studies should use standardized cutoff values for defining CMT/hypodontia and also standard methods for sampling and diagnosis. Future meta-analyses should include studies on orthodontic/dental patients as well, since due to the ethical concerns regarding X-ray exposure, epidemiological studies are unlikely affordable. Sampling from orthodontic patients might be preferable over dental patients or pediatric dentistry patients. This is because CMT results of orthodontic samples were closer to the epidemiological samples. However, it might be recommended to sample from both simultaneously, as their roles in biasing the prevalence are opposite of each other. Studies should not enroll children younger than 12 years. There seems to be no limit over the maximum age at least as long as positive extraction history is an exclusion criterion. It is recommended to adopt sufficiently large samples (based on power calculations) because of its obvious advantages. But since observers might miss some cases in such samples, two or more examiners should judge large samples to reduce or eliminate the corresponding false negative error. There seems to be no strong publication bias for accepting higher CMT prevalence rates.

Abbreviations

CMT

Congenital missing of teeth.

Footnotes

Competing interests

The author declares that he has no competing interest.

Author’s contributions

The conception, design, reviews, statistical analyses, interpretations, drafting, and preparation of this article were carried out by the author.

References

  • 1.Altug-Atac AT, Erdem D. Prevalence and distribution of dental anomalies in orthodontic patients. Am J Orthod Dentofacial Orthop. 2007;131:510–4. doi: 10.1016/j.ajodo.2005.06.027. [DOI] [PubMed] [Google Scholar]
  • 2.De Coster PJ, Marks LA, Martens LC, Huysseune A. Dental agenesis: genetic and clinical perspectives. J Oral Pathol Med. 2009;38:1–17. doi: 10.1111/j.1600-0714.2008.00699.x. [DOI] [PubMed] [Google Scholar]
  • 3.Goya HA, Tanaka S, Maeda T, Akimoto Y. An orthopantomographic study of hypodontia in permanent teeth of Japanese pediatric patients. J Oral Sci. 2008;50:143–50. doi: 10.2334/josnusd.50.143. [DOI] [PubMed] [Google Scholar]
  • 4.Bäckman B, Wahlin YB. Variations in number and morphology of permanent teeth in 7-year-old Swedish children. Int J Pediatr Dent. 2001;11:11–7. doi: 10.1046/j.1365-263x.2001.00205.x. [DOI] [PubMed] [Google Scholar]
  • 5.Endo T, Ozoe R, Kubota M, Akiyama M, Shimooka S. A survey of hypodontia in Japanese orthodontic patients. Am J Orthod Dentofacial Orthop. 2006;129:29–35. doi: 10.1016/j.ajodo.2004.09.024. [DOI] [PubMed] [Google Scholar]
  • 6.Castaldi CR, Bodnarchuk A, MacRae PD, Zacherl WA. Incidence of congenital anomalies in permanent teeth of a group of Canadian children aged 6-9. J Can Dent Assoc (Tor) 1966;32:154–9. [PubMed] [Google Scholar]
  • 7.Helm S. Malocclusion in Danish children with adolescent dentition: an epidemiologic study. Am J Orthod. 1968;54:352–66. doi: 10.1016/0002-9416(68)90304-7. [DOI] [PubMed] [Google Scholar]
  • 8.McKibben DR, Brearley LJ. Radiographic determination of the prevalence of selected dental anomalies in children. ASDC J Dent Child. 1971;28:390–8. [PubMed] [Google Scholar]
  • 9.Thilander B, Myrberg N. The prevalence of malocclusion in Swedish schoolchildren. Scand J Dent Res. 1973;81:12–21. doi: 10.1111/j.1600-0722.1973.tb01489.x. [DOI] [PubMed] [Google Scholar]
  • 10.Bergström K. An orthopantomographic study of hypodontia, supernumeraries and other anomalies in school children between the ages of 8-9 years. An epidemiological study. Swed Dent J. 1977;1:145–57. [PubMed] [Google Scholar]
  • 11.Brook AH. Dental anomalies of number, form and size: their prevalence in British school children. J Int Assoc Dent Child. 1974;5:37–53. [PubMed] [Google Scholar]
  • 12.Locht S. Panoramic radiographic examination of 704 Danish children aged 9-10 years. Community Dent Oral Epidemiol. 1980;8:375–80. doi: 10.1111/j.1600-0528.1980.tb01311.x. [DOI] [PubMed] [Google Scholar]
  • 13.Johannsdottir B, Wisth PJ, Magnusson TE. Prevalence of malocclusion in 6-year-old Icelandic children. Acta Odontol Scand. 1997;55:398–402. doi: 10.3109/00016359709059206. [DOI] [PubMed] [Google Scholar]
  • 14.Salem G. Prevalence of selected dental anomalies in Saudi children from Gizan region. Community Dent Oral Epidemiol. 1989;17:162–3. doi: 10.1111/j.1600-0528.1989.tb00014.x. [DOI] [PubMed] [Google Scholar]
  • 15.Pemberton TJ, Das P, Patel PI. Hypodontia: genetics and future perspectives. Braz J Oral Sci. 2005;4:695–709. [Google Scholar]
  • 16.Lynham A. Panoramic radiographic survey of hypodontia in Australian Defence Force recruits. Aust Dent J. 1990;35:19–22. doi: 10.1111/j.1834-7819.1990.tb03021.x. [DOI] [PubMed] [Google Scholar]
  • 17.Nik-Hussein NN. Hypodontia in the permanent dentition: a study of its prevalence in Malaysian children. Aust Orthod J. 1989;11:93–5. [PubMed] [Google Scholar]
  • 18.Amini F, Rakhshan V, Babaei P. Prevalence and pattern of hypodontia in the permanent dentition of 3374 Iranian orthodontic patients. Dent Res J (Isfahan) 2012;9:245–50. [PMC free article] [PubMed] [Google Scholar]
  • 19.Moon HS, Choi SC, Choung PH. Hypodontia and hyperdontia of permanent teeth in Korean schoolchildren. Cleft Lip and Palate Assoc. 2001;4:19–27. [Google Scholar]
  • 20.Dolder E. Deficient dentition. Dent Pract Dent Rec. 1936;57:142–3. [Google Scholar]
  • 21.Werther R, Rothenberg F. Anodontia: a review of its etiology with presentation of a case. Am J Orthod. 1939;25:61–81. [Google Scholar]
  • 22.Byrd ED. Incidence of supernumerary and congenitally missing teeth. J Dent Child. 1943;10:84–6. [Google Scholar]
  • 23.Ma C. Statistical observation of morphological and numerical teeth anomalies in the teeth of Japanese. Shikagaku Zasshi. 1949;6:248–56. [Google Scholar]
  • 24.Okamoto O, Mori O, Morimoto M, Nakao N, Miyakawa E. A statistical and genetic study related to congenital missing teeth. Shika Gakuho. 1951;5:8–10. [Google Scholar]
  • 25.Terasaki T, Shiota K. Congenital absence of teeth. Nihon Kokyuki Gakkai Zasshi. 1954;3:88–93. [Google Scholar]
  • 26.Tsutsui H, Yoshida Y. Clinical statistical study on supernumerary teeth and congenital absence of teeth. Kokubyo Gakkai Zasshi. 1955;22:44–8. [Google Scholar]
  • 27.Grahnén H. Hypodontia in the permanent dentition: a clinical and genetical investigation. Odont Revy. 1956;7:1–100. [Google Scholar]
  • 28.Clayton JM. Congenital dental anomalies occurring in 3557 children. J Dent Child. 1956;23:206–8. [Google Scholar]
  • 29.Lind V. Medfödda antalsvariationer i permanenta dentitionen. Odont Revy. 1959;10:176–89. [PubMed] [Google Scholar]
  • 30.Glenn F. Incidence of congenitally missing permanent teeth in a private pedodontic practice. ASDC J Dent Child. 1961;28:317–20. [Google Scholar]
  • 31.Gimnes H. En frekvensundersøkelse over hypodonti hos skolebarn i Oslo, med saerlig henblikk på forekomst av bilateral hypodonti av 2. premolar i underkjeven. Nor Tannlaegeforen Tid. 1963;73:141–8. [Google Scholar]
  • 32.Volk A. Über die Häufigkeit des Vorkommens von fehlenden Zahnanlagen. Schweiz Monatsschr Zahnmed. 1963;73:320–34. [Google Scholar]
  • 33.Niswander JD, Sujaku C. Congenital anomalies of teeth in Japanese children. Am J Phys Anthropol. 1963;21:569–74. doi: 10.1002/ajpa.1330210413. [DOI] [PubMed] [Google Scholar]
  • 34.Glenn FB. A consecutive six-year study of the prevalence of congenitally missing teeth in private pedodontic practice of two geographically separated areas. ASDC J Dent Child. 1964;3:264–70. [Google Scholar]
  • 35.Rosenzweig KA, Garbarski D. Numerical aberrations in the permanent teeth of grade school children in Jerusalem. Am J Phys Anthropol. 1965;23:277–83. doi: 10.1002/ajpa.1330230315. [DOI] [PubMed] [Google Scholar]
  • 36.Rose JS. A survey of congenitally missing teeth, excluding third molars, in 6000 orthodontic patients. Dent Pract Dent Rec. 1966;17:107–14. [PubMed] [Google Scholar]
  • 37.Horowitz JM. Aplasia and malocclusion: a survey and appraisal. Am J Orthod. 1966;52:440–53. doi: 10.1016/0002-9416(66)90122-9. [DOI] [PubMed] [Google Scholar]
  • 38.Blayney J, Hill I. Congenitally missing teeth. J Am Dent Assoc. 1967;74:298–9. doi: 10.14219/jada.archive.1970.0151. [DOI] [PubMed] [Google Scholar]
  • 39.Davies PL. Agenesis of teeth of the permanent dentition: a frequency study in Sydney schoolchildren. Aust Dent J. 1968;13:146–50. doi: 10.1111/j.1834-7819.1968.tb02254.x. [DOI] [PubMed] [Google Scholar]
  • 40.Muller TP, Hill IN, Peterson AC, Blayney JR. A survey of congenitally missing permanent teeth. J Am Dent Assoc. 1970;81:101–7. doi: 10.14219/jada.archive.1970.0151. [DOI] [PubMed] [Google Scholar]
  • 41.Haavikko K. Hypodontia of permanent teeth. An orthopantomographic study. Suom Hammaslaak Toim. 1971;67:219–25. [PubMed] [Google Scholar]
  • 42.Egermark-Eriksson I, Lind V. Congenital numerical variation in the permanent dentition. D. Sex distribution of hypodontia and hyperodontia. Odontol Revy. 1971;22:309. [PubMed] [Google Scholar]
  • 43.Hanaoka H, Yamauchi K, Kawasoko S, Imada Y. [Anomalies in number of teeth of orthodontic patients. 3. Relationship to malocclusion] Nippon Kyosei Shika Gakkai Zasshi. 1972;31:162. [PubMed] [Google Scholar]
  • 44.Eidelman E, Chosack A, Rosenzweig KA. Hypodontia: prevalence amongst Jewish populations of different origin. Am J Phys Anthropol. 1973;39:129–33. doi: 10.1002/ajpa.1330390113. [DOI] [PubMed] [Google Scholar]
  • 45.Ravn JJ. Nielsen LA [Orthopantomographic study of supernumerary teeth and aplasia among 1530 Copenhagen school children] Tandlaegebladet. 1973;77:12–22. [PubMed] [Google Scholar]
  • 46.Hunstadbraten K. Hypodontia in the permanent dentition. ASDC J Dent Child. 1973;40:115–7. [PubMed] [Google Scholar]
  • 47.Bachmann H. Die Häufigkeit von Nichtanlagen bleibender Zähne (ausgenommen der Weisheitszähne). Ergebnisse der Auswertung von 8694 Orthopantogrammen 9-10 Jährigen Schulkinder aus Zürich, dissertation. Zürich: University of Zürich; 1974. [Google Scholar]
  • 48.Wisth PJ, Thunold K, Böe OE. Frequency of hypodontia in relation to tooth size and dental arch width. Acta Odontol Scand. 1974;32:201–6. doi: 10.3109/00016357409002548. [DOI] [PubMed] [Google Scholar]
  • 49.Thompson GW, Popovich F. Probability of congenitally missing teeth: results in 1,191 children in the Burlington Growth centre in Toronto. Community Dent Oral Epidemiol. 1974;2:26–32. doi: 10.1111/j.1600-0528.1974.tb01790.x. [DOI] [PubMed] [Google Scholar]
  • 50.Magnússon TE. An epidemiologic study of dental space anomalies in Icelandic schoolchildren. Community Dent Oral Epidemiol. 1977;5:292–300. doi: 10.1111/j.1600-0528.1977.tb01017.x. [DOI] [PubMed] [Google Scholar]
  • 51.Nakahara M, Okada S, Tani H. [A survey of congenitally missing permanent teeth in Hokkaido] Koku Eisei Gakkai Zasshi. 1977;27:21. doi: 10.5834/jdh.27.21. [DOI] [PubMed] [Google Scholar]
  • 52.Maklin M, Dummett CO, Jr, Weinberg R. A study of oligodontia in a sample of New Orleans children. ASDC J Dent Child. 1979;46:478–82. [PubMed] [Google Scholar]
  • 53.Rølling S. Hypodontia of permanent teeth in Danish schoolchildren. Scand J Dent Res. 1980;88:365–9. doi: 10.1111/j.1600-0722.1980.tb01240.x. [DOI] [PubMed] [Google Scholar]
  • 54.Davis PJ. Hypodontia and hyperdontia of permanent teeth in Hong Kong schoolchildren. Community Dent Oral Epidemiol. 1987;15:218–20. doi: 10.1111/j.1600-0528.1987.tb00524.x. [DOI] [PubMed] [Google Scholar]
  • 55.Ishizuka K, Sasaki T, Imai R, Nakamura N, Yoshida T, Anabuki M, Tashiro M, Maeda K, Uchida Y, Inoue K. Abnomalies of teeth which affects the orthodontic treatment. Nichidai Shigaku. 1988;62:584–95. [Google Scholar]
  • 56.Lai PY, Seow WK. A controlled study of the association of various dental anomalies with hypodontia of permanent teeth. Pediatr Dent. 1989;11:291–6. [PubMed] [Google Scholar]
  • 57.Lo Muzio L, Mignogna MD, Bucci P, Sorrentino F. Statistical study of the incidence of agenesis in a sample of 1529 subjects. Minerva Stomatol. 1989;38:1045–51. [PubMed] [Google Scholar]
  • 58.Ignelzi MA, Jr, Fields HW, Vann WF., Jr Screening panoramic radiographs in children: prevalence data and implications. Pediatr Dent. 1989;11:279–85. [PubMed] [Google Scholar]
  • 59.Burden D, Connolly I. Radiographic study of hypodontia and other anomalies in orthodontic patients. J Dent Res. 1989;68:295. [Google Scholar]
  • 60.Renkerová M, Badura S, Manicová H, Jambor J. A contribution to anomalous number of teeth in children in the Zilina District. Praktické zubní lékar?ství. 1989;37:12. [PubMed] [Google Scholar]
  • 61.al-Emran S. Prevalence of hypodontia and developmental malformation of permanent teeth in Saudi Arabian schoolchildren. Br J Orthod. 1990;17:115–8. doi: 10.1179/bjo.17.2.115. [DOI] [PubMed] [Google Scholar]
  • 62.Yanagida I, Mori S. Statistical studies on numerical anomalies of teeth in children using orthopantomograms - congenital hypodontia. Osaka Daigaku Shigaku Zasshi. 1990;35:580–93. [PubMed] [Google Scholar]
  • 63.Dechkunakorn S, Chaiwat J, Sawaengkit P. Congenital absence and loss of teeth in an orthodontic patient group. J Dent Assoc Thai. 1990;40:165. [PubMed] [Google Scholar]
  • 64.O'Dowling IB, McNamara TG. Congenital absence of permanent teeth among Irish school-children. J Ir Dent Assoc. 1990;36:136–8. [PubMed] [Google Scholar]
  • 65.Legonic M, Ceranic I, Cehich A. Anomalies in the number of permanent teeth in orthodontic patients in 2 localities in Croatia. Schweiz Monatsschr Zahnmed. 1990;100:286–90. [PubMed] [Google Scholar]
  • 66.Polastri F, Cerato E, Gallesio C. The clinico-radiological assessment of dental anomalies with real and apparent numerical defects. Minerva Stomatol. 1991;40:415–23. [PubMed] [Google Scholar]
  • 67.Watanabe K, Motoyoshi M, Fukui R, Chang K, Namba Akira SM. A study on incidence of congenital missing of teeth among orthodontics patients. Nihon Univ Dent J. 1992;66:1029–1033. [Google Scholar]
  • 68.Cua-Benward GB, Dibaj S, Ghassemi B. The prevalence of congenitally missing teeth in class I, II, III malocclusions. J Clin Pediatr Dent. 1992;17:15–7. [PubMed] [Google Scholar]
  • 69.Aasheim B, Ogaard B. Hypodontia in 9-year-old Norwegians related to need of orthodontic treatment. Scand J Dent Res. 1993;101:257–60. doi: 10.1111/j.1600-0722.1993.tb01115.x. [DOI] [PubMed] [Google Scholar]
  • 70.Ogita S, Ogita M, Yamamoto T, Yanase H, Kondo YKY. The appearance of supernumerary teeth and congenitally missing teeth in 6299 Japanese pediatric patients. Aichi Gakuin Dent Sci. 1995;33:19–27. [Google Scholar]
  • 71.Cuairán RV, Gaitan ZL, Hernández MA. Agenesia dental en una muestra de pacientes ortodónticos del Hospital Infantil de México. ADM. 1996;53:211–5. [Google Scholar]
  • 72.Peltola JS, Wolf J, Mannik A, Russak S, Seedre T, Sirkel M, Vink M. Radiographic findings in the teeth and jaws of 14- to 17-year-old Estonian schoolchildren in Tartu and Tallinn. Acta Odontol Scand. 1997;55:31–5. doi: 10.3109/00016359709091938. [DOI] [PubMed] [Google Scholar]
  • 73.Tsai SJ, King NM. A catalogue of anomalies and traits of the permanent dentition of southern Chinese. J Clin Pediatr Dent. 1998;22:185–94. [PubMed] [Google Scholar]
  • 74.Ghaznawi HI, Daas H, Salako NO. A clinical and radiographic survey of selected dental anomalies and conditions in a Saudi Arabian population. 1999. [Google Scholar]
  • 75.Varela M, Arrieta P, Ventureira C. Non-syndromic concomitant hypodontia and supernumerary teeth in an orthodontic population. Eur J Orthod. 2009;31:632–7. doi: 10.1093/ejo/cjp046. [DOI] [PubMed] [Google Scholar]
  • 76.Hirukawa K, Iwata R, Kurosawa M, Kondo T, Goto S. Statistical investigation about the prevalence of congenitally missing permanent teeth. Orthodontic Waves. 1999;58:49–56. [Google Scholar]
  • 77.Ng'ang'a RN, Ng'ang'a PM. Hypodontia of permanent teeth in a Kenyan population. East Afr Med J. 2001;78:200–3. doi: 10.4314/eamj.v78i4.9063. [DOI] [PubMed] [Google Scholar]
  • 78.Gabris K, Tarjan I, Csiki P, Konrad F, Szadeczky B, Rozsa N. Prevalence of congenital hypodontia in the permanent dentition and its treatment. Fogorv Sz. 2001;94:137–40. [PubMed] [Google Scholar]
  • 79.Nordgarden H, Jensen JL, Storhaug K. Reported prevalence of congenitally missing teeth in two Norwegian counties. Community Dent Health. 2002;19:258–61. [PubMed] [Google Scholar]
  • 80.Al-Nakib LH, Younis WH. Orthopantomographic survey of hypodontia among Iraqi orthodontic patients. J Coll Dent. 2002;4:74. [Google Scholar]
  • 81.Osuji OO, Hardie J. Dental anomalies in a population of Saudi Arabian children in Tabuk. Saudi Dent J. 2002;14:11–4. [Google Scholar]
  • 82.Silva MR. Radiographic assessment of congenitally missing teeth in orthodontic patients. Int J Pediatr Dent. 2003;13:112–6. doi: 10.1046/j.1365-263x.2003.00436.x. [DOI] [PubMed] [Google Scholar]
  • 83.Fekonja A. Hypodontia in orthodontically treated children. Eur J Orthod. 2005;27:457–60. doi: 10.1093/ejo/cji027. [DOI] [PubMed] [Google Scholar]
  • 84.Albashaireh ZS, Khader YS. The prevalence and pattern of hypodontia of the permanent teeth and crown size and shape deformity affecting upper lateral incisors in a sample of Jordanian dental patients. Community Dent Health. 2006;23:239–43. [PubMed] [Google Scholar]
  • 85.Gábris K, Fábián G, Kaán M, Rózsa N, Tarján I. Prevalence of hypodontia and hyperdontia in paedodontic and orthodontic patients in Budapest. Community Dent Health. 2006;23:80–2. [PubMed] [Google Scholar]
  • 86.Sisman Y, Uysal T, Gelgor IE. Hypodontia. Does the prevalence and distribution pattern differ in orthodontic patients? Eur. J Dent. 2007;1:167–73. [PMC free article] [PubMed] [Google Scholar]
  • 87.Galluccio G, Pilotto A. Genetics of dental agenesis: anterior and posterior area of the arch. Eur Arch Paediatr Dent. 2008;9:41–5. doi: 10.1007/BF03321595. [DOI] [PubMed] [Google Scholar]
  • 88.Kuchler EC, Risso PA, Costa Mde C, Modesto A, Vieira AR. Studies of dental anomalies in a large group of school children. Arch Oral Biol. 2008;53:941–6. doi: 10.1016/j.archoralbio.2008.04.003. [DOI] [PubMed] [Google Scholar]
  • 89.Chung CJ, Han JH, Kim KH. The pattern and prevalence of hypodontia in Koreans. Oral Dis. 2008;14:620–5. doi: 10.1111/j.1601-0825.2007.01434.x. [DOI] [PubMed] [Google Scholar]
  • 90.Al-Ajwadi SAM. An orthopantomographic study of hypodontia in permanent teeth of Iraqi patients. Med Dent J. 2009;6:139–4. [Google Scholar]
  • 91.Peker I, Kaya E, Darendeliler-Yaman S. Clinic and radiographical evaluation of non-syndromic hypodontia and hyperdontia in permanent dentition. Med Oral Patol Oral Cir Bucal. 2009;14:e393–7. [PubMed] [Google Scholar]
  • 92.Uslu O, Akcam MO, Evirgen S, Cebeci I. Prevalence of dental anomalies in various malocclusions. Am J Orthod Dentofacial Orthop. 2009;135:328–35. doi: 10.1016/j.ajodo.2007.03.030. [DOI] [PubMed] [Google Scholar]
  • 93.Durrani OK, Zulfiqar K, Bashir U, Shamsher M. Prevalence of tooth agenesis in orthodontic patients at Islamic International Dental Hospital. Pakistan Orthod J. 2010;2:48–51. [Google Scholar]
  • 94.Guttal KS, Naikmasur VG, Bhargava P, Bathi RJ. Frequency of developmental dental anomalies in the Indian population. Eur J Dent. 2010;4:263–9. [PMC free article] [PubMed] [Google Scholar]
  • 95.Ajami B, Shab ZM, Afzal Aghaei M, Mehrjerdian MC. Prevalence and pattern of congenital missing teeth in a group of Iranian adolescents. J Dent Shiraz Univ Med Sci. 2010;10:40–4. [Google Scholar]
  • 96.Celikoglu M, Kazanci F, Miloglu O, Oztek O, Kamak H, Ceylan I. Frequency and characteristics of tooth agenesis among an orthodontic patient population. Med Oral Patol Oral Cir Bucal. 2010;15:e797–801. doi: 10.4317/medoral.15.e797. [DOI] [PubMed] [Google Scholar]
  • 97.Tallón-Walton V, Nieminen P, Arte S, Carvalho-Lobato P, Ustrell-Torrent JM, Manzanares-Céspedes MC. An epidemiological study of dental agenesis in a primary health area in Spain: estimated prevalence and associated factors. Med Oral Patol Oral Cir Bucal. 2010;15:e569––74. doi: 10.4317/medoral.15.e569. [DOI] [PubMed] [Google Scholar]
  • 98.Vahid-Dastjerdi E, Borzabadi-Farahani A, Mahdian M, Amini N. Non-syndromic hypodontia in an Iranian orthodontic population. J Oral Sci. 2010;52:455–61. doi: 10.2334/josnusd.52.455. [DOI] [PubMed] [Google Scholar]
  • 99.Aljazi Hussain AJ, Abdullah Mohammad A: A study on dento/skeletal discrepancies and dental anomalies in a sample of Saudi orthodontic patients. King Saud University; 2010. [Thesis]
  • 100.Aktan A, Kara I, Sener I, Bereket C, Ay S, Çiftçi M. Radiographic study of tooth agenesis in the Turkish population. Oral Radiol. 2010;26:95–100. [Google Scholar]
  • 101.Kositbowornchai S. Prevalence and distribution of dental anomalies in pretreatment orthodontic Thai patients. Khon Kaen Univ Dent J. 2011;13:92–100. [Google Scholar]
  • 102.Kim YH. Investigation of hypodontia as clinically related dental anomaly: prevalence and characteristics. ISRN Dent. 2011;2011:246135. doi: 10.5402/2011/246135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Lee JH, Yang BH, Lee SM, Kim YH, Shim HW, Chung HS. A study on the prevalence of dental anomalies in Korean dental-patients. Korean J Orthod. 2011;41:346–53. [Google Scholar]
  • 104.Gupta SK, Saxena P, Jain S, Jain D. Prevalence and distribution of selected developmental dental anomalies in an Indian population. J Oral Sci. 2011;53:231–8. doi: 10.2334/josnusd.53.231. [DOI] [PubMed] [Google Scholar]
  • 105.Behr M, Proff P, Leitzmann M, Pretzel M, Handel G, Schmalz G, Driemel O, Reichert TE, Koller M. Survey of congenitally missing teeth in orthodontic patients in Eastern Bavaria. Eur J Orthod. 2011;33:32–6. doi: 10.1093/ejo/cjq021. [DOI] [PubMed] [Google Scholar]
  • 106.Shetty P, Adyanthaya A, Adyanthaya S, Sreelatha SV. The prevalence of hypodontia and supernumerary teeth in 2469 school children of the Indian population: an epidemiological study. Indian J Stomatol. 2012;3:150–2. [Google Scholar]
  • 107.Cantekin K, Dane A, Miloglu O, Kazanci F, Bayrakdar S, Celikoglu M. Prevalence and intra-oral distribution of agenesis of permanent teeth among Eastern Turkish children. Eur J Paediatr Dent. 2012;13:53–6. [PubMed] [Google Scholar]
  • 108.Gonzalez-Allo A, Campoy MD, Moreira J, Ustrell J, Pinho T. Tooth agenesis in a Portuguese population. Int Orthod. 2012;10:198–210. doi: 10.1016/j.ortho.2012.03.001. [DOI] [PubMed] [Google Scholar]
  • 109.Afify AR, Zawawi KH. The prevalence of dental anomalies in the western region of Saudi Arabia. ISRN Dent. 2012;2012:837270. doi: 10.5402/2012/837270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Shimizu T, Maeda T. Prevalence and genetic basis of tooth agenesis. Jpn Dent Sci Rev. 2009;45:52–8. [Google Scholar]
  • 111.Murdock S, Lee JY, Guckes A, Wright JT. A costs analysis of dental treatment for ectodermal dysplasia. J Am Dent Assoc. 2005;136:1273–6. doi: 10.14219/jada.archive.2005.0343. [DOI] [PubMed] [Google Scholar]
  • 112.Wu CC-L, Wong RW-K, Hägg U. A review of hypodontia: the possible etiologies and orthodontic, surgical and restorative treatment options - conventional and futuristic. Hong Kong Dent J. 2007;4:113–21. [Google Scholar]
  • 113.Rune B, Sarnäs KV. Tooth size and tooth formation in children with advanced hypodontia. Angle Orthod. 1974;44:316–21. doi: 10.1043/0003-3219(1974)044<0316:TSATFI>2.0.CO;2. [DOI] [PubMed] [Google Scholar]
  • 114.Gomes RR, da Fonseca JAC, Paula LM, Faber J, Acevedo AC. Prevalence of hypodontia in orthodontic patients in Brasilia, Brazil. Eur J Orthod. 2010;32:302–6. doi: 10.1093/ejo/cjp107. [DOI] [PubMed] [Google Scholar]
  • 115.Larmour CJ, Mossey PA, Thind BS, Forgie AH, Stirrups DR. Hypodontia - a retrospective review of prevalence and etiology. Part I. Quintessence Int. 2005;36:263–70. [PubMed] [Google Scholar]
  • 116.Khosravanifard B, Rakhshan V, Raeesi E. Factors influencing attractiveness of soft tissue profile. Oral Surg Oral Med Oral Pathol Oral Radiol. 2013;115:29–37. doi: 10.1016/j.oooo.2012.03.021. [DOI] [PubMed] [Google Scholar]
  • 117.Polder BJ, Van't Hof MA, Van der Linden FPGM, Kuijpers-Jagtman AM. A meta-analysis of the prevalence of dental agenesis of permanent teeth. Community Dent Oral Epidemiol. 2004;32:217–26. doi: 10.1111/j.1600-0528.2004.00158.x. [DOI] [PubMed] [Google Scholar]
  • 118.Nunn JH, Carter NE, Gillgrass TJ, Hobson RS, Jepson NJ, Meechan JG, Nohl FS. The interdisciplinary management of hypodontia: background and role of paediatric dentistry. Br Dent J. 2003;194:245–51. doi: 10.1038/sj.bdj.4809925. [DOI] [PubMed] [Google Scholar]
  • 119.Brook AH. A unifying aetiological explanation for anomalies of human tooth number and size. Arch Oral Biol. 1984;29:373–8. doi: 10.1016/0003-9969(84)90163-8. [DOI] [PubMed] [Google Scholar]
  • 120.Mattheeuws N, Dermaut L, Martens G. Has hypodontia increased in Caucasians during the 20th century? A meta-analysis. Eur J Orthod. 2004;26:99–103. doi: 10.1093/ejo/26.1.99. [DOI] [PubMed] [Google Scholar]
  • 121.Sheikhi M, Sadeghi MA, Ghorbanizadeh S. Prevalence of congenitally missing permanent teeth in Iran. Dent Res J (Isfahan) 2012;9:S105–11. [PMC free article] [PubMed] [Google Scholar]
  • 122.Ajami BA, Shabzendedar M, Mehrjerdian M. Prevalence of hypodontia in nine- to fourteen-year-old children who attended the Mashhad School of Dentistry. Indian J Dent Res. 2010;21:549–51. doi: 10.4103/0970-9290.74215. [DOI] [PubMed] [Google Scholar]
  • 123.Tavajohi-Kermani H, Kapur R, Sciote JJ. Tooth agenesis and craniofacial morphology in an orthodontic population. Am J Orthod Dentofacial Orthop. 2002;122:39–47. doi: 10.1067/mod.2002.123948. [DOI] [PubMed] [Google Scholar]
  • 124.Sterzik G, Steinbicker V, Karl N. The etiology of hypodontia. Fortschr Kieferorthop. 1994;55:61–9. doi: 10.1007/BF02174358. [DOI] [PubMed] [Google Scholar]
  • 125.Silverman NE, Ackerman JL. Oligodontia: a study of its prevalence and variation in 4032 children. ASDC J Dent Child. 1979;46:470–7. [PubMed] [Google Scholar]
  • 126.Salama FS, Abdel-Megid FY. Hypodontia of primary and permanent teeth in a sample of Saudi children. Egypt Dent J. 1994;40:625–32. [PubMed] [Google Scholar]
  • 127.Ringqvist M, Thilander B. The frequency of hypodontia in an orthodontic material. Sven Tandlak Tidskr. 1969;62:535–41. [PubMed] [Google Scholar]
  • 128.Schalk-van der Weide Y, Beemer FA, Faber JA, Bosman F. Symptomatology of patients with oligodontia. J Oral Rehabil. 1994;21:247–61. doi: 10.1111/j.1365-2842.1994.tb01141.x. [DOI] [PubMed] [Google Scholar]
  • 129.Ogaard B, Krogstad O. Craniofacial structure and soft tissue profile in patients with severe hypodontia. Am J Orthod Dentofacial Orthop. 1995;108:472–7. doi: 10.1016/s0889-5406(95)70047-1. [DOI] [PubMed] [Google Scholar]
  • 130.Ghaznawi HI, Daas H, Salako NO. A clinical and radiographic survey of selected dental anomalies and conditions in a Saudi Arabian population. Saudi Dent J. 1999;11:8–13. [Google Scholar]

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