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Association between missing lateral incisor side and gender. 

Association between missing lateral incisor side and gender. 

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Objective This study aims to estimate the prevalence of congenitally missing lateral incisors in a sample of 2662 dental patients in Palestine. Methods A total of 2662 digital panoramic radiographs were retrospectively examined for the presence of congenitally missing permanent lateral incisors. The radiographs were obtained from the archival reco...

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... test revealed no significant asso- ciation between gender and maxillary lateral incisor agenesis (P > .05) ( Table 3). The prevalence for missing maxillary lat- eral incisors in all the cases was 1.91% (Table 2). ...

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... The congenital missing permanent teeth, excluding third molars, affects 3-10% of individuals, or almost one in 10-12 of the population (1)(2)(3). Congenital maxillary lateral incisor missing (CMLIM) has an important place in this percentage; in fact, according to many studies, the maxillary lateral incisors represent the teeth most frequently missing congenitally following the third molars (4)(5)(6)(7)(8)(9). In permanent dentition, congenitally missing two or one of the maxillary lateral incisors causes a discrepancy in the maxillary dentition and, consequently, in the mandibular dentition and presents serious aesthetic problems, especially in the anterior region (10). ...
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Aim: The aim of the study was to compare the trabecular changes in alveolar bone structure after the treatment of congenital maxillary lateral incisor missing (CMLIM) with space-opening and -closure methods by fractal dimension (FD) analysis. Material and Methods: The study included 48 patients and three groups were formed: control (Group 1), space-opening (Group 2), and space-closure groups (Group 3). FD analysis was performed on panoramic images taken before (T0) and after (T1) treatment in the area of interest of trabecular alveolar bone determined in the distal apical region of the maxillary central incisor. For inter-group comparisons, the Kruskal-Wallis test was employed, while the Wilcoxon test was utilized for intra-group comparisons. The statistical significance was determined as p0.05). In Group 2, a significant decrease in FD values was observed during the T1 period compared to T0, whereas Group 3 showed a significant increase (p
... Partial hypodontia may be subdivided into oligodontia, the congenital absence of six or more teeth (third molars are not included), and hypodontia, the congenital absence of fewer than six teeth (third molars are not included). [4,5] Hypodontia is the most common form of tooth agenesis. [6,7] The prevalence of hypodontia varies between different ethnic groups, from 2.8% to 11.3%, depending on the population studied. ...
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A BSTRACT Objectives This retrospective study aimed to determine the prevalence of congenitally missing mandibular second premolars. Materials and Methods A total of 1,843 radiographs were collected from five different cities in Palestine. Two experienced dentists independently examined the panoramic radiographs and demographic data (age and gender). Results Among the 1,843 radiographs, 1,039 were for females (57.37%) and 804 were for males (43.63%); 13 cases had at least one congenitally mandibular second premolar. The prevalence of congenitally missing mandibular second premolars in the study population was 0.7%. There was no significant association between gender and mandibular second premolar agenesis. Unilateral agenesis was more common than bilateral, and the left side had more cases of congenitally missing mandibular second premolars than the right side. Conclusions The prevalence of congenitally missing mandibular second premolars in this study population was 0.7%, within the range reported in other populations.
... Other genetic diseases like cleft lip and palate, Downs' syndrome, hypohidrotic dysplasia, ectodermal dysplasia, Witkop syndrome, holoprosencephaly, incontinentia pigmenti, Van der Woude syndrome, and Rieger syndrome would also lead to hypodontia. 7 Numerous studies have assessed the prevalence of congenitally missing teeth among different study populations, as follows. According to a systematic review and meta-analysis done by Khalaf et al., the highest prevalence of hypodontia was found in Africa (13.5%) followed by Europe (7%), Asia, and Australia (6.3%). ...
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... The permanent maxillary lateral incisor is the most common missing tooth (not including the third molars) (Fauzi et al., 2019;Mani et al., 2014;Nik-Hussein, 1989;Shakirah Said et al., 2017) and can contribute to malocclusion (Caterini et al., 2017). Two-thirds of the missing maxillary lateral incisor were unilateral, while the remaining one-third were bilateral (Arandi & Mustafa, 2018). A study on the Malaysian population found that more missing teeth observed at the maxilla and on the right side (Fauzi et al., 2019), although there was another study found that missing permanent maxillary lateral incisor were more commonly occurred on the left side (Arandi & Mustafa, 2018). ...
... Two-thirds of the missing maxillary lateral incisor were unilateral, while the remaining one-third were bilateral (Arandi & Mustafa, 2018). A study on the Malaysian population found that more missing teeth observed at the maxilla and on the right side (Fauzi et al., 2019), although there was another study found that missing permanent maxillary lateral incisor were more commonly occurred on the left side (Arandi & Mustafa, 2018). was 3.77% (Sahoo et al., 2019;Swarnalatha et al., 2020). ...
... Meanwhile, the prevalence of missing permanent maxillary lateral incisor among hypodontia orthodontic patients were 26.5% (Acev & Gjorgova, 2014), 19.8% (Kim, 2011), and 17.8% (Gracco et al., 2017;Zakaria et al., 2021). However, the prevalence of missing permanent maxillary lateral incisor was found to be lower among non-orthodontic populations; 1.91% (Arandi & Mustafa, 2018), and 2.56% (Musaed et al., 2019). ...
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... Its occurrence can vary among different ethnic groups. This condition can be unilateral or bilateral and may occur either on its own or as part of a genetic disorder [5]. ...
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... Finally, the normal spacing of teeth is used to help differentiate between tooth loss and congenital absence. In cases of tooth agenesis, nearby teeth frequently drift mesially to partly fill in the resulting gap (Arandi and Mustafa 2018), justifying the inclusion of regular spacing in ablation studies (e.g., Lee 2017; Pietrusewsky and Douglas 1993;Tayles 1996). Though multiple studies discuss patterns in ablation, and we discuss it below, our methodological focus here is on the characteristics of ablation itself. ...
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Dientes con modificaciones intencionales dan un registro duradero de identidades pasadas, pero su identificación en especímenes arqueológicos ha sido inconsistente. Esta investigación evalúa los criterios de diagnóstico comunes para identificar la ablación dental intencional por medio de la prueba de casos de falsos positivos de ablación en un grupo de control de primates no humanos, donde no se esperan casos verdaderos de ablación dental. El autor principal observó la dentición de 849 primates no humanos de la División de Mamíferos del Museo Nacional de Historia Natural, incluso los grandes simios, los simios menores y los monos del Viejo Mundo de cuerpo relativamente grande. Se seleccionó una muestra para un análisis más profundo basado en la ausencia de dientes antemortem y la historia del espécimen. De una muestra de once investigaciones publicada, se eligieron siete metodologías diferentes que utilizan combinaciones de seis criterios de diagnóstico para la identificación de la ablación dental. Para determinar qué combinaciones de criterios pueden haber identificado falsamente la ablación dental en estos especímenes si fueran humanos, se analizó el grupo de control de primates no humanos en función de la pérdida de dientes anteriores, la falta de enfermedad, la simetría de la ausencia de dientes, la curación completa del hueso alveolar, la falta de evidencia para traumatismos y el espacio normal entre los dientes. Todos los métodos de análisis produjeron resultados falsos positivos, muchos de los Dientes con modificaciones intencionales dan un registro duradero de identidades pasadas, pero su identificación en especímenes arqueológicos ha sido inconsistente. Esta investigación evalúa los criterios de diagnóstico comunes para identificar la ablación dental intencional por medio de la prueba de casos de falsos positivos de ablación en un grupo de control de primates no humanos, donde no se esperan casos verdaderos de ablación dental. El autor principal observó la dentición de 849 primates no humanos de la División de Mamíferos del Museo Nacional de Historia Natural, incluso los grandes simios, los simios menores y los monos del Viejo Mundo de cuerpo relativamente grande. Se seleccionó una muestra para un análisis más profundo basado en la ausencia de dientes antemortem y la historia del espécimen. De una muestra de once investigaciones publicada, se eligieron siete metodologías diferentes que utilizan combinaciones de seis criterios de diagnóstico para la identificación de la ablación dental. Para determinar qué combinaciones de criterios pueden haber identificado falsamente la ablación dental en estos especímenes si fueran humanos, se analizó el grupo de control de primates no humanos en función de la pérdida de dientes anteriores, la falta de enfermedad, la simetría de la ausencia de dientes, la curación completa del hueso alveolar, la falta de evidencia para traumatismos y el espacio normal entre los dientes. Todos los métodos de análisis produjeron resultados falsos positivos, muchos de los 2–17% del grupo de control de primates no humanos, con las tasas más altas de falsos positivos cuando la simetría o el espacio normal no se incluyeron como criterios de discriminación. Este trabajo demuestra la necesidad de metodologías exhaustivas y descriptivas para la replicabilidad. También ilumina la importancia de la simetría y el espacio entre dientes como criterios diagnósticos para evitar falsos positivos.
... In addition, there seems to be a difference in the pattern of lateral incisor agenesis on the right and left sides. Studies have reported that the prevalence and pattern of right or left lateral incisor agenesis vary by race and ethnicity [30][31][32]. Individuals with unilateral lateral incisor agenesis had smaller teeth in the missing sides than teeth in the nonmissing sides, and smaller teeth than individuals without tooth agenesis [33,34]. ...
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Background Sex dimorphism has been implicated in oral health differences and the pathogenesis of oral diseases, such as tooth agenesis, periodontal disease, dental caries, and tooth loss. Tooth agenesis (TA) is one of the most common developmental anomalies in humans, and its prevalence and patterns are different across ethnic groups. The aim of this study was to investigate the phenotypes and sex-associated patterns of nonsyndromic tooth agenesis (TA) in Thai dental patients. Methods One thousand ninety panoramic radiographs were examined. One hundred and one subjects (37 males, 64 females, 15–20 years-old) with nonsyndromic TA were evaluated. Differences in TA prevalence between groups were analyzed using the chi-square or Fisher exact test. Results The TA prevalence, excluding third molars, was 9.3% and more frequently found in the mandible compared with the maxilla. The maxilla demonstrated a higher prevalence of first premolar agenesis than the mandible ( P = 0.012), while the mandible had a higher prevalence of second premolar agenesis than the maxilla ( P = 0.031). There were significantly more males missing one tooth than females, however, there were more females missing two or more teeth than males ( P = 0.042). A missing maxillary left lateral incisor was significantly more frequent in males ( P = 0.019), while a missing mandibular right lateral incisor was more frequent in females ( P = 0.025). In females, the pattern of two mandibular lateral incisors agenesis was the most common and significantly present in females more than males ( P = 0.015). In contrast, the pattern of one mandibular left lateral incisor agenesis was only observed in males and significantly found in males more than females ( P = 0.047). Conclusions We demonstrate sex-associated differences in nonsyndromic tooth agenesis. The prevalence of single tooth agenesis was higher in males, while that of two or more teeth agenesis was higher in females. We found different patterns of lateral incisor agenesis between males and females.
... In maxillary lateral incisor agenesis, Bassiouny et al. [11] reported that 4.9% of an orthodontic group were affected. Other studies performed on different population samples found lower prevalence values of between 1.15% and 2.4% [12][13][14], while a study of twins reported a prevalence of 2.5% [15]. Bilateral agenesis of upper lateral incisors appears to be more common in some populations than unilateral agenesis [3], while other populations show a higher prevalence of unilateral cases [12,13]. ...
... Other studies performed on different population samples found lower prevalence values of between 1.15% and 2.4% [12][13][14], while a study of twins reported a prevalence of 2.5% [15]. Bilateral agenesis of upper lateral incisors appears to be more common in some populations than unilateral agenesis [3], while other populations show a higher prevalence of unilateral cases [12,13]. Hypodontia of maxillary lateral incisors can be present alone, as a mild form of hypodontia (one or two missing teeth), or associated with missing premolars, in moderate forms of hypodontia (three to five missing teeth) or as part of many missing teeth, including molars, in severe forms of hypodontia (six or more missing teeth) [16,17]. ...
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(1) Background: Hypodontia has a multifactorial aetiology, in which genetic factors are a major component. Associated with this congenital absence, the formed teeth may show differences in size and shape, which may vary with the specific genetic variants and with the location of the missing teeth. The aims of the present study were to investigate a specific variant of MSX1, derive morphometric tooth measurements in a sample of patients with isolated maxillary lateral incisor agenesis and matched controls, and model the findings. (2) Methods: Genotyping of the MSX1 rs8670 genetic variant and morphometric measurements with a 2D image analysis method were performed for 26 hypodontia patients and 26 matched controls. (3) Results: The risk of upper lateral incisor agenesis was 6.9 times higher when the T allele was present. The morphometric parameters showed significant differences between hypodontia patients and controls and between the unilateral and bilateral agenesis cases. The most affected crown dimension in the hypodontia patients was the bucco-lingual dimension. In crown shape there was significant variation the Carabelli trait in upper first molars. (4) Conclusions: The MSX1 rs8670 variant was associated with variations in morphological outcomes. The new findings for compensatory interactions between the maxillary incisors indicate that epigenetic and environmental factors interact with this genetic variant. A single-level directional complex interactive network model incorporates the variations seen in this study.