- Original article
- Open Access
Asynchronous dentofacial development and dental crowding: a cross-sectional study in a contemporary sample of children in France
© Yan-Vergnes et al.; licensee BioMed Central Ltd. 2013
- Received: 2 July 2013
- Accepted: 5 November 2013
- Published: 19 November 2013
The causes of dental crowding are not fully understood, but it may result from an evolutionary trend towards reduced facial volume, without a proportional reduction in tooth sizes. Most previous studies conducted among modern humans have revealed a very low or non-existent correlation between tooth size and jaw size. Cross-comparison between dental age and facial skeletal age could help to provide better knowledge of the dynamic process of dental crowding. The primary objective of this research was to study the synchronism of dental maturation and skeletal facial growth in a sample of modern children living in France. The secondary objective was to assess the link between dentofacial asynchronism and dental crowding.
The random sample comprised 28 subjects (16 girls, 12 boys). Mean chronological age was 13.5 years (±2.1; range 9.2–17.6). Mean dental age was 14.2 years (±2.8; range 7.5–17) and mean facial skeletal age was 12.8 years (±2.6, range 7–22). In the estimations of dental age and facial skeletal age, there was no evidence of systematic bias. There were 10 subjects (9 girls, 1 boy) with asynchronous dentofacial development. Finally, there were 13 subjects (8 girls, 5 boys) with dental crowding. A significant association was found between delayed facial skeletal growth/advanced dental maturation and dental crowding (P = 0.01).
Dental maturation and facial growth are not necessarily synchronous. Further understanding of the interactions between dental maturation and facial growth could have crucial implications in biological anthropology, as well as for the clinical practice of orthodontists. From an anthropological perspective, this study suggests that asynchronous dentofacial development could, at least partially, explain the frequency of dental crowding in modern populations.
- Facial Growth
- Tooth Movement
- Centroid Size
- Tooth Size
- Pubertal Growth Spurt
Research in physiological anthropology is essential to a better understanding of past and present human populations. In facial anthropology, the study of the timing of facial growth and its relationship to dental maturation is of special interest for the purpose of improving knowledge about human evolution (paleoanthropology) , for medical purposes (orthodontic care)  and for legal purposes (age estimation in forensic anthropology) . A condition related to both facial development and dental maturation is dental crowding.
Dental crowding can be defined as a discrepancy between tooth and jaw sizes that results in malposition and/or rotation of teeth . Dental crowding is not a disease in itself but can be considered a condition that can lead to or promote diseases  such as periodontal disease , dental caries  or temporomandibular joint dysfunction . Nowadays, the prevalence of dental crowding is estimated to range between 30% and 60% [9–12]. It is one of the most frequent reasons why people consult an orthodontist, especially given the high aesthetic demand expressed by patients .
The causes of dental crowding are still not fully understood, but they may rooted in an evolutionary trend toward reduced facial volume without a proportional reduction in tooth size . Most previous studies conducted among primates have revealed a very low or nonexistent correlation between tooth size and jaw size [15, 16]. It has been shown that, as human populations transitioned from a hunter-gatherer lifestyle to an agricultural one, there was a consistent shift toward a shorter and broader mandible . Thus, dental crowding could occur as a result of the increased processing of modern foods and thus a reduced need for powerful masticatory action .
Independently of the causes of dental crowding, several studies have examined the extent to which tooth and jaw sizes contribute to the condition. It has been found that groups of individuals with dental crowding have smaller dental arch dimensions than noncrowded groups [4, 19]. McKeown  found a stronger correlation between arch size and dental crowding than between tooth size and dental crowding. These observations are controversial, however, and varying numbers of confirming and refuting observations are available. For example, a recent study suggested that tooth size could play a greater role than jaw size in the development of dental crowding .
To the best of our knowledge, most previous studies that have assessed discrepancies between tooth size and jaw size have used raw clinical and/or cephalometric measurements without focusing on the physiological stages of dental maturation or stages of facial growth. Stages of dental maturation in humans have been the subject of extensive research, and Demirjian et al.’s method  for age estimation based on teeth is now widely used in both anthropology and forensics [23–26]. More recently, a method was devised to estimate the age of children by using the centroid size of their facial skeleton .
Cross-comparison between dental age and facial skeletal age could help to provide better knowledge of the dynamic process of dental crowding. Our hypothesis is that, at the individual level, dental crowding could be the result of an asynchronism between dental maturation and facial growth.
The primary aim of our present study was to examine the synchronism of dental maturation and facial growth in a sample of modern children. The secondary aim was to assess the link between dentofacial asynchronism and dental crowding.
Study design and sampling methods
We conducted a retrospective cross-sectional study based on computed tomography (CT) scans of a contemporaneous cohort of children of various origins who lived in the Toulouse, France, area. The sample was drawn from a database of CT scans taken between 2001 and 2010 in the Neuroradiology Unit of the Clinique Pasteur, Toulouse, and Toulouse University Hospital. CT scans of the children had been taken because of trauma, impacted or residual teeth, inflammation in the maxillary sinuses or neonatal distress. The whole database is securely hosted in the Anthropology Laboratory of Molecular Imaging and Synthesis (UMR5288, CNRS). A French institutional review board provided ethical approval of the study . The CT data were anonymous and numbered. Each number was entered into an Excel file with, exclusively, the date of birth, the date of the CT scan and the child’s sex.
To be included in the present analysis, participants had to be younger than 18 years of age, have all their mandibular permanent teeth (erupted or not, except the wisdom teeth), have a Demirjian stage  of at least 6 for mandibular permanent incisors and at least 7 for the first mandibular permanent molars (to allow for space analysis using Nance’s principles ) and have complete radiographic acquisition to permit assessment of dental age, facial skeletal age and dental crowding.
From the initial database, sampling was performed in two phases. Participants were first randomly selected from the initial database, then inclusion criteria were applied to incrementally produce the working database until the sample size calculated a priori was attained (see Statistical considerations).
Facial skeletal age was estimated using a method previously developed to assess the skeletal age of children, based on the centroid size of the face and derived from the three-dimensional coordinates of anatomical landmarks . The anatomical locations of bilateral landmarks (mental foramen, anterior opening of the infraorbital canal, anterior opening of the supraorbital canal, supraorbital fissure at the level of the optic foramen and round foramina) were selected using AMIRA 3D analysis software (version 5.2.2; FEI Visualization Sciences Group, Mérignac, France), and centroid sizes were calculated using morphologika software . The centroid size is a measure of size uncorrelated with all pure shape changes . The facial skeletal age was calculated using least squares linear regression (with distinction between boys and girls and between children younger or older than 10 years) . Chronological and facial skeletal ages were rounded down to the nearest semester. A child was considered as presenting delayed facial skeletal growth if his or her chronological age was strictly greater than the estimation of his or her facial skeletal age (that is, greater than and not equal to).
Dental age was estimated by using a previously described method . A panoramic projection of teeth from Digital Imaging and Communications in Medicine, or DICOM, files allowed Demirjian’s stages  of the right hemimandible of each child  to be assessed. Estimation of dental age was based on Bayesian predictions . Chronological and dental ages were rounded down to the nearest semester. A child was considered as presenting advanced dental maturation if his or her chronological age was strictly less than the estimation of dental age.
Regarding synchronism, a child was considered as revealing asynchronous dentofacial development if he or she had (1) delayed facial skeletal growth and advanced dental maturation (DS/AD) or (2) advanced facial skeletal growth and delayed dental maturation (AS/DD). Thus, we distinguished two types of asynchronous dentofacial development: the DS/AD type and the AS/DD type. By definition, we considered all other children as having synchronous dentofacial development.
Space analysis required a comparison between the amount of space actually available for the alignment of the teeth and the amount of space necessary to align them properly . Space conditions were calculated following Nance’s principles  using OsiriX imaging software (version 4.0; http://www.osirix-viewer.com/). Individual mesiodistal crown lengths of all mandibular permanent teeth, exclusive of molars, were measured. The cumulative mesiodistal crown lengths defined the space required. Mandibular arch perimeter was measured from the mesial surface of the first permanent molar to the mesial surface of the opposite molar, thus defining the available space. Next, the difference between the space available and the space required was calculated (expressed in millimeters). A child was considered to have dental crowding if the space required was strictly greater than the space available.
The null hypothesis was that the proportion of children with dental crowding was the same in both groups, with or without DS/AD asynchronous dentofacial development.
Sample size was calculated using the normal approximation to the arcsine transformation of the binomial distribution . The sample size required to detect a difference in proportion of 50% between the two groups at the significance level of 5% with a power of 80% is 28. Groups were compared with a two-sided Fisher’s exact test.
Statistical procedures for estimating dental age and facial skeletal age have been detailed in previous articles [25, 27]. As described in these articles, estimation of dental age and facial skeletal age were performed using different algorithms for boys and girls.
Dental age and facial skeletal age were compared with chronological age using the Bland–Altman plotting method . In this method, the differences between the age estimate and the chronological age are plotted against the averages of age estimates and chronological ages. We used the Bland–Altman plot to investigate any possible relationship of the discrepancies between age estimations and chronological age (that is, proportional bias). Proportional bias occurs when age estimation and chronological age do not agree equally throughout the range of measurements. Horizontal lines were drawn at the mean difference and at the limits of agreement (mean difference ±1.96). The software packages used were Scilab software (version 5.3.3; Scilab Enterprises, Versailles, France) for estimating dental age using the Bayesian approach and R version 2.15.1 software (The R Project for Statistical Computing; http://www.r-project.org/) for all statistical analyses.
Visualization of cases
Descriptive analysis of the sample
There were 10 children (9 girls and 1 boy) with DS/AD asynchronous dentofacial development, and only one (a boy) with AS/DD asynchronous dentofacial development. There were 13 children (8 girls and 5 boys) with dental crowding.
Cross-tabulation of the presence or absence of delayed facial skeletal growth and advanced dental maturation asynchronous dentofacial development a against the presence or absence of dental crowding
DS/AD asynchronous dentofacial development
The results of this study indicate that dental maturation and facial growth are not necessarily synchronous. In our present study, we found a significant association between DS/AD and dental crowding (P = 0.01). Although an observed association does not imply causation , this result is concordant with the existing body of studies in which researchers investigated the possible etiology of dental crowding. More precisely, our study favors the theory that dental crowding could be a consequence of low masticatory stresses, not only at the human evolution level but also at the individual level. This theory is congruent with the hypothesis that facial shape differences observed between agricultural and hunter-gatherer populations are significantly attributable to phenotypic plasticity rather than to natural selection only . Carlson and Van Gerven argued that changes in masticatory function and diet had so reduced chewing stress that the jaws did not develop to a sufficient size to hold all the teeth . In previous localized comparisons of hunter-gatherer and farming populations, significant changes occurring in the masticatory apparatus were found to occur within a relatively short time period, suggesting developmental plasticity or rapid selection. The delayed facial skeletal growth observed in some individuals in our study sample could be related to inadequate chewing stresses, thus generating insufficient strain for mandibular growth in relation to overall tooth size . This could lead to reduced alveolar and corpus lengths, as well as reduced skeletal facial volume, thus diminishing the space for complete dental eruption . Several arguments published in the literature can be put forward to support this interpretation of our results. For example, a recent study showed that there was an association between mandibular size and number of molars retained in occlusion, with smaller mandibular dimensions found in individuals retaining fewer occluding molars . A study of nonhuman primates found that hyraxes raised on cooked food had significantly less growth (approximately 10%) in the ventral (inferior) and posterior portions of the face . Although some authors have suggested that dental crowding is more frequent in modern populations than among ancient populations , diachronic changes in archaeological settings have been reported only minimally . In fact, evidence from the eastern Mediterranean, Southeast Asia and the American Southeast indicates that increased dental crowding rates coincide with a shift to agricultural societies and softer, westernized diets .
Rose and Roblee favored the explanation that reduced chewing stress in childhood produced jaws that were too small for the teeth, despite the ubiquitous trend in tooth size reduction . Kelley and Larsen suggested a strong association of alveolar bone growth with the functional stimulation of chewing forces. This work included measurements of bite-force variation between generations of Eskimos and animal studies showing changes in mandibular growth of rats and primates between groups that ate hard or soft diets . Diet-associated reduction in chewing stress was found to result in decreased growth of the mandibular and maxillary arches and, in animal studies, in both facial reduction and increased malocclusion in the low-force groups .
These current explanations contrast with Begg’s suggestions, published in the mid-1950s, that interstitial attrition caused by chewing forces reduced the mesiodistal lengths of all teeth so that they could fit within the jaw . This hypothesis has always failed to explain early incisor crowding as well as crowding in children and adolescents prior to an age when attrition becomes advanced . However, some researchers today still maintain that dental crowding might be genetic in origin and might not be caused by excessive tooth size or changes in environmental factors (masticatory activity) . Normando and colleagues recently emphasized the role of heredity in the occurrence of dental crowding , suggesting a highly polygenic basis for complex traits such as human craniofacial and dentition morphology and development .
An unexpected finding of our present study is that DS/AD asynchronous dentofacial development was more frequent among girls than among boys (relative ratio: (9/16)/(1/12) ≈ 7). Moreover, the only case of AS/DD asynchronous dentofacial development was found in a boy.
This finding could not be attributed to the well-documented systematic differences between boys and girls regarding the timing of dental or skeletal maturation, because age estimations were performed separately on each sex subset within the database, in accordance with the methods we used. Several explanations could be suggested. First, our study was designed primarily to assess the link between dentofacial asynchronism and dental crowding. This unexpected finding could be explained by a study design inadequate to test the hypothesis of a difference in AS/DD asynchronism between girls and boys. Second, we cannot reject a negative potentiation between delayed facial skeletal growth and advanced dental maturation among girls or a positive potentiation among boys. The reasons for these putative synergistic effects remain unclear, but they could be related to sexual dimorphism. Sexual dimorphism of the adult modern human facial skeleton, including the mandible, has been noted in diverse populations . Further studies are required to search for the link between sex and dentofacial asynchronism.
Our findings could have practical clinical implications. Knowledge of the facial skeletal growth and dental maturation status could be a useful tool in orthodontic treatment planning. Further development of tools for treatment planning could allow the orthodontist to integrate the assessment of dentofacial asynchronism into daily decision-making. For example, severe dental crowding in a child with DS/AD is not likely to lead to the same treatment plan as dental crowding in a child of the same age with AS/DD. In the first case, growth stimulation should be considered, whereas in the second, serial extraction or dental stripping might be a better option. Prediction of facial growth velocity and percentage of facial growth remaining can be important in orthodontic treatment planning  and may be essential if the purpose of the prediction is to take advantage of it during orthodontic treatment , especially in the presence of dental crowding. An accurate prediction of the pubertal growth spurt might be beneficial in the treatment of some types of malocclusion associated with skeletal disorders . In some cases, less tooth movement may be required, and growth may be an ally; under other clinical conditions, tooth movement will have a predominant role, depending on whether the growth pattern is favorable or unfavorable . All individuals undergo a pubertal growth spurt, but there are noteworthy differences in onset, duration, velocity and amount of growth . Although a significant correlation has been found between skeletal maturation and facial growth spurt at the population level , it is well-known that the bones of the face are formed by intramembranous ossification without cartilaginous precursors. Thus, growth of the face may be regulated by factors other than those responsible for growth of the long bones . It remains challenging to personalize orthodontic treatment-planning at the individual level, because genetic factors and differences between sex and ethnic group are also associated with the onset, duration, intensity and end of the growth spurt . All of these factors are likely to interact with each other and have differential effects on facial growth, statural growth or biological maturation. Moreover, the findings of our present study could support the hypothesis that dental maturation may not be linked directly to facial or mandibular growth . Again, despite a significant correlation between dental maturation and bone age found in many studies of various populations [54–56], such correlations are generally considered to be moderate at best . This could explain why dental development indicators are not reliable predictors of an individual’s stage of skeletal development.
The present study has several limitations. We considered the chronological age as the reference for estimating both dental age and facial skeletal age. The concepts of “advanced” and “delayed” maturation are relative to the mean values of the population from which the estimation methods have been developed. The population analyzed in our study comprised a random sample of the database used to generate the method for estimating facial skeletal age. Both methods used in this analysis are freely available [25, 27] and need to be studied in other populations. Additionally, it might be of special interest to analyze the factors associated with the occurrence of dental crowding among people with asynchronous dentofacial development. A longitudinal study could be conducted with analysis using a life-course approach, taking into account the determinants of dental crowding from a biopsychosocial perspective.
Dental maturation and facial growth are not necessarily synchronous. At the individual level, in the presence of dental crowding, orthodontic treatment planning could benefit from a personalized assessment of dental maturation versus skeletal facial growth, but practical tools need to be developed and validated at the population level. From an anthropological perspective, our present study suggests that asynchronous dentofacial development could at least partially explain the frequency of dental crowding in modern populations of children.
We are grateful to Dr Jacques Treil, and thank Susan Becker for revision of the English text. We also thank the two anonymous reviewers for invaluable comments relating to this article.
- Lieberman D: The Evolution of the Human Head. 2011, Cambridge, MA: Belknap PressGoogle Scholar
- Enlow DH, Hans MG: Essentials of Facial Growth. 1996, Philadelphia: SaundersGoogle Scholar
- Senn DR, Weems RA: Manual of Forensic Odontology. 2013, Boca Raton, FL: CRC PressView ArticleGoogle Scholar
- Howe RP, McNamara JA, O’Connor KA: An examination of dental crowding and its relationship to tooth size and arch dimension. Am J Orthod. 1983, 83: 363-373. 10.1016/0002-9416(83)90320-2.View ArticlePubMedGoogle Scholar
- Lombardi AV: The adaptive value of dental crowding: a consideration of the biologic basis of malocclusion. Am J Orthod. 1982, 81: 38-42. 10.1016/0002-9416(82)90286-X.View ArticlePubMedGoogle Scholar
- Geiger AM: Malocclusion as an etiologic factor in periodontal disease: a retrospective essay. Am J Orthod Dentofacial Orthop. 2001, 120: 112-115. 10.1067/mod.2001.114537.View ArticlePubMedGoogle Scholar
- Hafez HS, Shaarawy SM, Al-Sakiti AA, Mostafa YA: Dental crowding as a caries risk factor: a systematic review. Am J Orthod Dentofacial Orthop. 2012, 142: 443-450. 10.1016/j.ajodo.2012.04.018.View ArticlePubMedGoogle Scholar
- Henrikson T, Ekberg EC, Nilner M: Symptoms and signs of temporomandibular disorders in girls with normal occlusion and class II malocclusion. Acta Odontol Scand. 1997, 55: 229-235. 10.3109/00016359709115422.View ArticlePubMedGoogle Scholar
- Šidlauskas A, Lopatienė K: The prevalence of malocclusion among 7–15-year-old Lithuanian schoolchildren. Medicina (Kaunas). 2009, 45: 147-152.Google Scholar
- Tausche E, Luck O, Harzer W: Prevalence of malocclusions in the early mixed dentition and orthodontic treatment need. Eur J Orthod. 2004, 26: 237-244. 10.1093/ejo/26.3.237.View ArticlePubMedGoogle Scholar
- Lew KK, Foong WC, Loh E: Malocclusion prevalence in an ethnic Chinese population. Aust Dent J. 1993, 38: 442-449. 10.1111/j.1834-7819.1993.tb04759.x.View ArticlePubMedGoogle Scholar
- Thilander B, Myrberg N: The prevalence of malocclusion in Swedish schoolchildren. Scand J Dent Res. 1973, 81: 12-21.PubMedGoogle Scholar
- Marques LS, Pordeus IA, Ramos-Jorge ML, Filogônio CA, Filogônio CB, Pereira LJ, Paiva SM: Factors associated with the desire for orthodontic treatment among Brazilian adolescents and their parents. BMC Oral Health. 2009, 9: 34-10.1186/1472-6831-9-34.PubMed CentralView ArticlePubMedGoogle Scholar
- Lundström A: The aetiology of crowding of the teeth (based on studies of twins and on morphological investigations) and its bearing on orthodontic treatment (expansion or extraction). Trans Eur Orthod Soc. 1951, 176-189.Google Scholar
- Plavcan JM, Daegling DJ: Interspecific and intraspecific relationships between tooth size and jaw size in primates. J Hum Evol. 2006, 51: 171-184. 10.1016/j.jhevol.2006.02.005.View ArticlePubMedGoogle Scholar
- Le Cabec A, Kupczik K, Gunz P, Braga J, Hublin JJ: Long anterior mandibular tooth roots in Neanderthals are not the result of their large jaws. J Hum Evol. 2012, 63: 667-681. 10.1016/j.jhevol.2012.07.003.View ArticlePubMedGoogle Scholar
- von Cramon-Taubadel N: Global human mandibular variation reflects differences in agricultural and hunter-gatherer subsistence strategies. Proc Natl Acad Sci U S A. 2011, 108: 19546-19551. 10.1073/pnas.1113050108.PubMed CentralView ArticlePubMedGoogle Scholar
- Normando D, Almeida MAO, Quintão CCA: Dental crowding. Angle Orthod. 2013, 83: 10-15. 10.2319/020112-91.1.View ArticlePubMedGoogle Scholar
- Golwalkar SA, Msitry KM: An evaluation of dental crowding in relation to the mesiodistal crown widths and arch dimensions. J Ind Orthod Soc. 2009, 43: 22-29.Google Scholar
- McKeown M: The diagnosis of incipient arch crowding in children. N Z Dent J. 1981, 77: 93-96.PubMedGoogle Scholar
- Poosti M, Jalali T: Tooth size and arch dimension in uncrowded versus crowded class I malocclusions. J Contemp Dent Pract. 2007, 8: 45-52.PubMedGoogle Scholar
- Demirjian A, Goldstein H, Tanner JM: A new system of dental age assessment. Hum Biol. 1973, 45: 211-227.PubMedGoogle Scholar
- Pelsmaekers B, Loos R, Carels C, Derom C, Vlietinck R: The genetic contribution to dental maturation. J Dent Res. 1997, 76: 1337-1340. 10.1177/00220345970760070201.View ArticlePubMedGoogle Scholar
- Liversidge HM, Speechly T: Growth of permanent mandibular teeth of British children aged 4 to 9 years. Ann Hum Biol. 2001, 28: 256-262. 10.1080/030144601300119070.View ArticlePubMedGoogle Scholar
- Braga J, Heuze Y, Chabadel O, Sonan NK, Gueramy A: Non-adult dental age assessment: correspondence analysis and linear regression versus Bayesian predictions. Int J Legal Med. 2005, 119: 260-274. 10.1007/s00414-004-0494-8.View ArticlePubMedGoogle Scholar
- Chaillet N, Nyström M, Demirjian A: Comparison of dental maturity in children of different ethnic origins: international maturity curves for clinicians. J Forensic Sci. 2005, 50: 1164-1174.View ArticlePubMedGoogle Scholar
- Braga J, Treil J: Estimation of pediatric skeletal age using geometric morphometrics and three-dimensional cranial size changes. Int J Legal Med. 2007, 121: 439-443. 10.1007/s00414-007-0170-x.View ArticlePubMedGoogle Scholar
- Nance HN: The limitations of orthodontic treatment: mixed dentition diagnosis and treatment. Am J Orthod. 1947, 33: 177-223.PubMedGoogle Scholar
- O’Higgins P, Jones N: Facial growth in Cercocebus torquatus: an application of three dimensional geometric morphometric techniques to the study of morphological variation. J Anat. 1998, 193: 251-272. 10.1046/j.1469-7580.1998.19320251.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Bookstein FL: Morphometric Tools for Landmark Data: Geometry and Biology. 1997, Cambridge, UK: Cambridge University PressGoogle Scholar
- Akhoondali H, Zoroofi RA, Shirani G: Fully automatic extraction of panoramic dental images from CT-scan volumetric data of the head. J Appl Sci. 2009, 9: 2106-2114. 10.3923/jas.2009.2106.2114.View ArticleGoogle Scholar
- Schirmer UR, Wiltshire WA: Manual and computer-aided space analysis: a comparative study. Am J Orthod Dentofacial Orthop. 1997, 112: 676-680. 10.1016/S0889-5406(97)70234-8.View ArticlePubMedGoogle Scholar
- Mace AE: Sample Size Determination. 1964, New York: Van Nostrand ReinholdGoogle Scholar
- Bland JM, Altman DG: Statistical methods for assessing agreement between two methods of clinical measurement. Lancet. 1986, 1: 307-310.View ArticlePubMedGoogle Scholar
- Bland JM, Altman DG: Correlation in restricted ranges of data. BMJ. 2011, 342: d556-10.1136/bmj.d556.View ArticlePubMedGoogle Scholar
- Carlson DS, Van Gerven DP: Masticatory function and post-Pleistocene evolution in Nubia. Am J Phys Anthropol. 1977, 46: 495-506. 10.1002/ajpa.1330460316.View ArticlePubMedGoogle Scholar
- Kaifu Y, Kasai K, Townsend GC, Richards LC: Tooth wear and the “design” of the human dentition: a perspective from evolutionary medicine. Am J Phys Anthropol Suppl. 2003, 122 (S37): 47-61. 10.1002/ajpa.10329.View ArticleGoogle Scholar
- Mays SA: Loss of molar occlusion and mandibular morphology in adults in an ancient human population consuming a coarse diet. Am J Phys Anthropol. 2013, 152: 383-392. 10.1002/ajpa.22362.View ArticlePubMedGoogle Scholar
- Lieberman DE, Krovitz GE, Yates FW, Devlin M: St Claire M: Effects of food processing on masticatory strain and craniofacial growth in a retrognathic face. J Hum Evol. 2004, 46: 655-677. 10.1016/j.jhevol.2004.03.005.View ArticlePubMedGoogle Scholar
- Corruccini RS: An epidemiologic transition in dental occlusion in world populations. Am J Orthod. 1984, 86: 419-426. 10.1016/S0002-9416(84)90035-6.View ArticlePubMedGoogle Scholar
- Larsen CS: Biological changes in human populations with agriculture. Annu Rev Anthropol. 1995, 24: 185-213. 10.1146/annurev.an.24.100195.001153.View ArticleGoogle Scholar
- Rose JC, Roblee RD: Origins of dental crowding and malocclusions: an anthropological perspective. Compend Contin Educ Dent. 2009, 30: 292-300.PubMedGoogle Scholar
- Advances in Dental Anthropology. Edited by: Kelley MA, Larsen CS. 1991, New York: Wiley-LissGoogle Scholar
- Begg PR: Stone Age man’s dentition: with reference to anatomically correct occlusion, the etiology of malocclusion, and a technique for its treatment. Am J Orthod. 1954, 40: 517-531. 10.1016/0002-9416(54)90103-7.View ArticleGoogle Scholar
- Mockers O, Aubry M, Mafart B: Dental crowding in a prehistoric population. Eur J Orthod. 2004, 26: 151-156. 10.1093/ejo/26.2.151.View ArticlePubMedGoogle Scholar
- Normando D, Faber J, Guerreiro JF, Quintão CCA: Dental occlusion in a split Amazon indigenous population: genetics prevails over environment. PLoS One. 2011, 6: e28387-10.1371/journal.pone.0028387.PubMed CentralView ArticlePubMedGoogle Scholar
- Carroll SB: Genetics and the making of Homo sapiens. Nature. 2003, 422: 849-857. 10.1038/nature01495.View ArticlePubMedGoogle Scholar
- Coquerelle M, Bookstein FL, Braga J, Halazonetis DJ, Weber GW, Mitteroecker P: Sexual dimorphism of the human mandible and its association with dental development. Am J Phys Anthropol. 2011, 145: 192-202. 10.1002/ajpa.21485.View ArticlePubMedGoogle Scholar
- Flores-Mir C, Nebbe B, Major PW: Use of skeletal maturation based on hand-wrist radiographic analysis as a predictor of facial growth: a systematic review. Angle Orthod. 2004, 74: 118-124.PubMedGoogle Scholar
- de Souza Araujo MT, de Alcantara C-SA: Jardim da Motta AF: Clinical and radiographic guidelines to predict pubertal growth spurt. Dental Press J Orthod. 2011, 16: 98-103. 10.1590/S2176-94512011000500015.View ArticleGoogle Scholar
- Houston WJ, Miller JC, Tanner JM: Prediction of the timing of the adolescent growth spurt from ossification events in hand-wrist films. J Orthod. 1979, 6: 145-152.View ArticleGoogle Scholar
- Bergersen EO: The male adolescent facial growth spurt: its prediction and relation to skeletal maturation. Angle Orthod. 1972, 42: 319-338.PubMedGoogle Scholar
- Coquerelle M, Bayle P, Bookstein FL, Braga J, Halazonetis DJ, Katina S, Weber GW: The association between dental mineralization and mandibular form: a study combining additive conjoint measurement and geometric morphometrics. J Anthropol Sci. 2010, 88: 129-150.PubMedGoogle Scholar
- Kumar S, Singla A, Sharma R, Virdi MS, Anupam A, Mittal B: Skeletal maturation evaluation using mandibular second molar calcification stages. Angle Orthod. 2012, 82: 501-506. 10.2319/051611-334.1.View ArticlePubMedGoogle Scholar
- Krailassiri S, Anuwongnukroh N, Dechkunakorn S: Relationships between dental calcification stages and skeletal maturity indicators in Thai individuals. Angle Orthod. 2002, 72: 155-166.PubMedGoogle Scholar
- Uysal T, Sari Z, Ramoglu SI, Basciftci FA: Relationships between dental and skeletal maturity in Turkish subjects. Angle Orthod. 2004, 74: 657-664.PubMedGoogle Scholar
- Morris JM, Park JH: Correlation of dental maturity with skeletal maturity from radiographic assessment: a review. J Clin Pediatr Dent. 2012, 36: 309-314.View ArticlePubMedGoogle Scholar
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.