Dental Anomalies and Muscle Segment Homeobox1 Gene Polymorphism in Non-syndromic Cleft Lip with or without Palate Children

Authors

  • Amel Elduhrahman B Elgali School of Dental Sciences, Health Campus, Universiti Sains Malaysia
  • Normastura Abd Rahman School of Dental Sciences, Health Campus, Universiti Sains Malaysia
  • Azlina Ahmad School of Dental Sciences, Health Campus, Universiti Sains Malaysia
  • Norliana Ghazali School of Dental Sciences, Health Campus, Universiti Sains Malaysia

DOI:

https://doi.org/10.22452/adum.vol30no4

Keywords:

Cleft lip , Cleft palate, Hypodontia, Mutation, Polymerase chain reaction

Abstract

This study aims to determine the prevalence of dental anomalies and MSX1 gene 799G>T polymorphism and its association with non-syndromic cleft lip with or without palate (NSCL±P) attending Hospital Universiti Sains Malaysia.  Clinical and radiological assessments on 37 NSCL±P patients and 80 non-cleft children were done to detect dental anomalies. The buccal cells were collected and polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) was used to identify polymorphism. NSCL±P was higher among males (54%) and mostly unilateral cleft lip and palate (51.3%). The prevalence of dental anomalies in morphology in NSCL±P was 18.9% (95% CI: 5.7%, 32.2%) and non-cleft was 6.3% (95% CI: 0.8%, 11.7%). Hypodontia in NSCL±P was 75% (95% CI: 61.2%, 90.2%) and non-cleft was 7.5% (95% CI: 1.6%, 13.4%). There was a significant association between NSCL±P and anomalies in morphology (P= 0.04; OR=3.5)) and number (P< 0.01; OR= 40). There was an absence of rare 799G>T polymorphism in all NSCL±P and non-cleft children indicating that all samples contain common 799G polymorphism. In conclusion, the prevalence of dental anomalies in morphology and number was significantly higher in NSCL±P compared to non-cleft children. However, it was not significantly associated with MSX1 799G>T polymorphism.

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Published

2023-12-24

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Section

Original/Research Article

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