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Volume 2012 (2012), Article ID 837270, 5 pages
The Prevalence of Dental Anomalies in the Western Region of Saudi Arabia
Division of Orthodontics, Faculty of Dentistry, King Abdulaziz University, P.O. Box 80209, Jeddah 21589, Saudi Arabia
Received 24 March 2012; Accepted 26 April 2012
Academic Editors: M. Behr, W. Bretz, F. Cairo, D. Drake, and O. Moses
Copyright © 2012 Ahmed R. Afify and Khalid H. Zawawi. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Objective. The aim of this cross-sectional study was to investigate the prevalence of dental anomalies that could be a cause of malocclusion in the western region of Saudi Arabia. Materials and Methods. A retrospective study of 878 digital orthopantomograms (OPGs) taken of patients, age ranging between 12 and 30 years, who presented to treatment at the Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia between 2002 and 2011. The OPGs and dental records were reviewed for congenitally missing teeth, supernumerary teeth, impactions, ectopic eruption, transposition, germination, fusion, dilacerations, taurodontism, dens in dent, and any other unusual conditions that can be assessed with OPG. Results. The prevalence of patient that exhibited at least one dental anomaly was 396 (45.1%) patients. The prevalence of congenitally missing teeth was 226 (25.7%), impacted teeth 186 (21.1%), dilacerated teeth 10 (1.1%), supernumerary teeth 3 (0.3%), odontoma 1 (0.1%), and taurodontism was also 1 case (0.1%) of the total radiographs reviewed. Conclusions. Congenitally missing teeth were found to be the most prevalent anomaly (25.7%), and the second frequent anomaly was impacted teeth (21.1%), whereas root dilacerations, supernumerary teeth, and taurodontism were the least frequent anomalies (1.1%, 0.3% and 0.1%, resp.).
Dental anomalies in tooth number, shape, and position usually result in problems in maxillary and mandibular arch length and occlusion, which may greatly influence orthodontic treatment planning. The etiology of these conditions is usually attributed to certain genes in addition to some etiological events in the prenatal and postnatal periods that may result in anomalies in tooth size, shape, position, number, and structure [1–5].
Congenitally missing teeth constitute the most common developmental anomaly of the human dentition, occurring in approximately 25% of the population, and the wisdom tooth represents the most affected tooth (20.7%) . Excluding third molars, the prevalence of tooth agenesis is approximately 4.3 to 7.8%, and the mandibular second premolars are the most commonly missing teeth, followed by the maxillary lateral incisors and maxillary second premolars . Ethnic background was found to have an effect on the prevalence of tooth agenesis. Epidemiological studies revealed a lower prevalence of agenesis in the Black race compared to the White race, while Asians showed increased tooth agenesis compared to Whites . Sexual differences were also reported in the prevalence of tooth agenesis, where women were more affected compared to men . The unilateral occurrence is predominant, except in the case of maxillary lateral incisor agenesis, where bilateral agenesis is more common. The primary etiological factor of tooth agenesis is attributed to genetics  where the prevalence is higher in families of affected patients . A mutation in the gene MSX1 of the chromosome 4 was identified in a family whose all members suffered from agenesis of second premolars and third molars . Additionally, in a study that included monozygotic and dizygotic twins, a high frequency of agreement for tooth agenesis in monozygotic twins was found, while pairs of dizygotic twins showed disagreement for this dental anomaly .
Impacted teeth play a significant role in the etiology of different types of malocclusions. The permanent maxillary canines develop close to nasal cavity, far from the dental arch, and, therefore, have the longest eruption path compared to other permanent teeth. In about 1.5% of population, the canines show an ectopic eruption path towards the palate . The orthodontic implication of this dental anomaly beside preventing the canines to erupt spontaneously, in a significant number of cases, could lead to root resorption of neighbouring teeth . Peck et al.  postulated that genetics are the essential etiological factor in the palatally displaced canines.
One or more dental anomalies can often be observed in the same patient. Studies on the patterns of association among seven types of dental anomalies in an untreated orthodontic population between the ages of 7 to 14 years found a significant reciprocal associations among five of the anomalies, a finding that suggests a common genetic origin. The prevalence of palatally displaced canine is greater in patients with microdontia. It was found that 34% of the patients with conical-shaped upper lateral incisors had palatally displaced canine . When studying the association of maxillary first molars’ agenesis with other dental anomalies in 32 Japanese orthodontic patients, the authors found that agenesis of maxillary first molars was associated with a higher prevalence of other permanent tooth agenesis . In another study, the prevalence of agenesis of permanent teeth was 13-fold higher in subjects with absent third molars compared to subjects in whom third molars were present [16, 17].
Many researchers investigated the prevalence of various dental anomalies but relatively little have related it to orthodontic treatment. Therefore, the aim of this study was to investigate the prevalence of dental anomalies that could be a cause of malocclusion in the western Region of Saudi Arabia.
2. Materials and Methods
A total of 1255 records of patients who attended the Faculty of Dentistry, King Abdulaziz University between 2002 and 2011 were screened. Only 878 records satisfied the inclusion criteria. Only the records of Saudi patients who were between the ages of 12 to 30 years were selected. The exclusion criteria included patients who exhibited one or more of the following: any disease, trauma, or fracture of the jaws that may affect the normal growth of permanent dentition. Records of patients who presented with hereditary condition or syndromes that could cause dental anomaly, such as Down’s syndrome or cleidocranial dysostosis were also rejected. Dental records and orthopantomograms (OPGs) were reviewed for the following dental anomalies: congenitally missing teeth (agenesis), supernumerary teeth, impaction, ectopic eruption, transposition, germination, fusion, dilacerations, taurodontism, dens in dente (Dens Evaginatus) and any other unusual condition. Digital orthopantomograms (OPGs) of these patients were examined in a standard manner under good lighting conditions, standardized screen brightness and resolution. The study was reviewed and approved by the Research Ethical Committee at the Faculty of Dentistry, King Abdulaziz University.
Data was analyzed comparing males and females. The differences between the groups were tested using the Chi-square test. The level of significance was set at 5% . The Statistical Package for Social Sciences (SPSS, version 11.01, Chicago, IL) was used.
A total of 878 records met the inclusion criteria and were reviewed and examined. Of these 430 were males (49.0%) and 448 were females (51.0%). The prevalence of patients who had at least one dental anomaly was 45.1% of the total sample examined. Table 1 shows the summary of the prevalence of dental anomalies found. A total of 226 (25.7%) patients had congenially missing teeth of which the third molar was missing in 185 patients (21.1%).
The prevalence of impaction was 21.2% (186 patients) and prevalence of third molar impaction was the highest (15.9%) compared to upper canine (3.3%), lower premolar (0.6%), and others (upper second premolar and lower second premolar, 1.4%).
The prevalence of dilacerations was 1.1%, supernumerary teeth was 0.3%, taurodontism was 0.01% as well as odontoma.
When comparing all these dental anomalies between females and males, showed that there were no significant differences between males and females with respect to the prevalence of all dental anomalies, .
Orthodontic patients have been reported to have high rates of dental anomalies [9, 12–14]. Inadequate consideration of these dental anomalies can complicate orthodontic treatment; therefore, their presence should be thoroughly investigated during orthodontic diagnosis and carefully considered during treatment planning.
This study was done to detect the prevalence of dental anomalies in the western region of Saudi Arabia that could be a cause of malocclusion. One can argue that the selected sample could only represent a limited population. The Faculty of Dentistry receives patients not only for the city of Jeddah but also from the surrounding suburban areas as well as neighboring cities. Therefore, it is fair to state that the selected sample could represent the geographic western region of Saudi Arabia. Dental anomalies may be expressed with different degrees of severity from the mildest developmental delay to the most severe tooth agenesis manifestation; dental anomalies may be expressed as microdontia, changes in dental morphology and ectopias . Several studies have suggested a genetic and hereditary background in the etiology of dental anomalies of number, size, position, as well as timing of development. This was derived from studies in families, monozygotic twins, and from the frequent observation of associations of certain dental anomalies [9–11, 14].
The prevalence of dental anomalies reported in this study was rather high, 45.1%. This could be attributed to a large extent to the anomalies of the wisdom teeth. A high prevalence of congenitally missing and impaction of wisdom teeth is reported in this study. One limitation to this finding is that the impactions were not classified (e.g., partial or fully impacted) and the angulation of impaction was not taken into consideration.
The association between the unilateral agenesis of the maxillary lateral incisor and the microdontia of the contralateral one, often observed clinically, well explains this condition. In this case, the same genetic defect, which determined the agenesis, has an incomplete expression in the opposite side of the dental arch, causing microdontia. However, the associations between the dental anomalies are not restricted to this usual example. There are many more interactions between different dental anomalies. The clinical implications are important because the early diagnosis of a given dental anomaly can alert the professional to the possible development of other associated dental anomalies in the same patient or family, permitting early diagnosis and timely orthodontic management.
The data in this study indicate the prevalence of tooth impaction is similar to the data reported in earlier studies while other studies report different rates. The current data showed that the incidence of impaction to be 21.2%, and this is somewhat higher than what was reported previously [18–22]. In this study, maxillary canines were the most commonly impacted teeth, excluding third molars. Furthermore, the prevalence of impacted cuspid was 3.3%, and this figure is similar to findings of Aydin et al.  and Zahrani  who reported 3.6% and 3.6% cuspid impaction, respectively. However, Fardi et al.  reported significantly lower figures in which he only observed 8.8% of cases exhibiting cuspid impaction.
Previous reports demonstrated the rarity of impacted cuspids in the mandible and this is also confirmed in the present study [19, 26–28]. In fact, none of the cases reviewed showed mandibular cuspid impacted. Grover and Lorton  examined 5,000 panoramic radiographs and found 142 cases having impacted cuspids in the maxilla (2.8%) and only 11 in the mandible, 0.2%. In another study of 1,000 Turkish patients, the incidence of maxillary cuspid impaction was 2.9%, while the incidence of impacted mandibular cuspid was 0.3% . Shah et al.  observed only eight impacted mandibular cuspids among 7,886 patients (0.1%). Early detection of impacted teeth is of paramount importance from a therapeutic point of view. Impacted teeth result in many complications, and their early detection is imperative.
Previous reports showed that the range of the prevalence of supernumerary teeth was 0.1–3.8% of the population [30–32]. The current finding, however, was 0.3%, a finding that is not in concert with what was reported by Fardi et al.  in which the prevalence of supernumerary teeth was 1.8%.
Several studies reported the incidence of the supernumerary teeth in different populations. Bäckman and Wahlin  conducted a clinical study by examining 739 Caucasian children and found 14 cases (1.9%) of at least one supernumerary tooth, and the majority of the supernumerary teeth reported were mesiodens. Salem  investigated the incidence of supernumerary teeth in a sample of 2,393 Saudi Arabian children and found that only 0.5% sample studied had at least one supernumerary tooth.
Several investigators indicated a higher prevalence of supernumerary teeth in males compared to females. In this study the male-to-female ratio was 1 : 2, which is in accord with the ratio reported for the Caucasians  but in disagreement with the ratios reported in other studies [25, 31, 33]. This could be due to the small number of observed supernumerary cases (i.e., 2 females and one male).
(i)Congenitally missing teeth were found to be the most prevalent anomaly (25.7%), and the second frequent anomaly was impacted teeth (21.1%).(ii)Root dilacerations, supernumerary teeth, and taurodontism were the least frequent anomalies observed (1.1%, 0.3%, and 0.1% resp.).(iii)There were no significant differences in the prevalence of different dental anomalies between males and females.
The authors are grateful to Drs.: Dalal Mahjoob, Eman Hefni, Farah Al-Juraifani, and Mohammed Al-Ulaiyan for their help during data collection.
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