Runt-related transcription factor 2 (RUNX2) plays important roles in osteoblast
differentiation, tooth development and chondrocyte maturation; hence its involvement in
craniofacial development is paramount. Mutation in RUNX2 is implicated with cleidocranial
dysplasia; a bone development disorder, while single nucleotide polymorphism (SNP) in RUNX2 is
associated with Class II/2 malocclusion. This study aimed to determine RUNX2 SNP of DNA marker
(rs6930053) in malocclusion patients from local population. (Copied from article).
PAX9 (Paired box 9) gene is one of the genes which play significant role during
craniofacial development. Single nucleotide polymorphism (SNP) in PAX9 has been associated with
Class II/Division 2 malocclusion (with or without hypodontia). However, the relationship between
PAX9 SNP marker (rs8004560) with mandibular prognathism (MP) has not been analysed, at least in
our local population. This study aimed to detect the presence of PAX9 (rs8004560) SNP in Class III
malocclusion patients (with MP) in the local population. (Copied from article).
Research into dental treatment via statistical perspective was unraveled through a relation between theoretical and experimental probability. This assessment of association was examined using statistical test over Confirmatory Factor Analysis (CFA) and Latent Class Analysis (LCA). Theoretical results of the prevailing difference between the direct and indirect upshot was verified through a technique known as integrated model by using Mplus® software package. The results expressively show that the dental treatment from the indirect effect has better performance than the direct effect. Besides that, there is a dramatic improvement of dental treatment from different type of malocclusion analysis. Three classes of different type of malocclusion analysis play an important role as mediator for demographic variable and type of dental treatment.
Non-syndromic tooth agenesis defined as developmental absence of more than one
tooth that appears as independent congenital oral trait. Its prevalence, pattern and distribution
rates vary by populations. The aim of this study was to identify the pattern and distribution of
tooth agenesis in permanent dentition among IIUM dental polyclinic patients. (Copied from article).
Evidence suggests that several genes; including MYO1H, play an important role in the
etiology of Class III malocclusion. Single nucleotide polymorphism (SNP) in marker rs10850110 (locus
12q24.11) within MYO1H gene has been associated with the incidence of mandibular prognathism
(MP). MYO is a class 1 myosin that is responsible for the synthesis of Matrilin-1; an important
protein involved in the formation of cartilage's extracellular matrix, hence is implicated in the
formation of mandibular condyle cartilage. This study aimed to detect the presence of MYO1H
(rs10850110) SNP and to determine its genotype and allele distribution in MP patient in the local
population. (Copied from article).
Polymorphism in PAX9 (rs8004560), a gene responsible for craniofacial and tooth development, is often associated with Class II/Div2 malocclusion. This study aimed to detect the presence of PAX9 SNP (rs8004560) and to determine its genotype and allele distribution in Class II skeletal base malocclusion, contributed by retrognathic mandible, in the local Malaysian population. The association of PAX9 SNP (rs8004560) with Class II skeletal base malocclusion was also determined. A case control study was performed on 30 samples; 15 from Class II skeletal base malocclusion, and 15 from Class I skeletal base subject as control. Cephalometric measurements were performed prior to saliva samples collection. Genomic DNA was extracted from unstimulated saliva of all subjects, and the DNA was amplified using specific primers for marker rs8004560, followed by genotyping by sequencing. SHEsis online software was used to analyse Hardy-Weinberg Equilibrium (HWE) for cases and controls. Allelic and genotypic frequencies were compared between cases and controls. Significant difference in allele frequency was observed within the group whereby G allele was over-represented in the analysed population (p0.05). Although no genetic association between PAX9 SNP (rs8004560) with Class II skeletal base malocclusion was observed, significant difference in allele frequency observed might provide some indication in the involvement of PAX9 polymorphism in Class II skeletal base malocclusion contributed by retrognathic mandible. Further research utilising larger sample size will be required in order to determine the role of PAX9 gene in the aetiology of Class II skeletal base malocclusion observed in the local Malaysian population.