Genetic Factors Involved in Mandibular Prognathism
Anna Doraczynska-Kowalik1, Kamil H Nelke, Wojciech Pawlak
1*Department of Genetics †Department of Maxillo-Facial Surgery, Wroclaw Medical University, Wroclaw, Poland.
The Journal of Craniofacial Surgery
|June 2, 2017
Summary
Mandibular prognathism, a skeletal Class III malocclusion, likely has a genetic basis. Research points to polygenic inheritance and identifies specific gene loci and candidate genes involved in its development.
Area of Science:
- Genetics
- Orthodontics
- Developmental Biology
Background:
- Mandibular prognathism is characterized by the mandible projecting forward.
- It is classified as a skeletal Class III pattern and Angle Class III malocclusion.
- The exact causes are unknown, but genetic, epigenetic, and environmental factors are suspected.
Purpose of the Study:
- To investigate the genetic and epigenetic factors contributing to mandibular prognathism.
- To identify potential gene loci and candidate genes associated with this condition.
Main Methods:
- Review of existing literature on twin studies, family segregation, and genetic linkage analyses.
- Identification of candidate genes and genes suspected in epigenetic regulation.
Main Results:
- Family and twin studies suggest significant genetic influence on mandibular prognathism.
- Linkage analyses identified significant loci on chromosomes 1p, 3q, 4p, 6q, 11q, 12q, 14q, and 19p.
- Candidate genes include MATN1, COL2A1, FGFR2, and growth hormone receptor, among others.
- Epigenetic regulation may involve genes such as MYH1, FOXO3, and RUNX2.
Conclusions:
- Mandibular prognathism likely follows a multifactorial or polygenic inheritance pattern.
- Specific chromosomal loci and numerous candidate genes are implicated in its etiology.
- Further research into these genetic and epigenetic factors is warranted.
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