Association between mandibular prognathism and Matrilin-1, bone morphogenic protein, Tyr67Asn, homeobox protein hox-A2, Rho-GTPase activating protein, and Myosin 1H genes in the Indian population
Mandibular prognathism (MP) patients present with aesthetic concerns and functional issues, including difficulties in mastication and pronunciation. Studies revealed that mandibular prognathism had definitive Mendelian inheritance patterns. This study aimed to ascertain distinct genetic markers associated with mandibular prognathism in individuals of Indian descent, focusing on exploring the prevalent genetic variations associated with certain genes. This study sought to identify the association of the following gene markers with mandibular prognathism: 1) Matrilin-1 (MATN1) (rs1065755), 2) Bone morphogenic protein 3 (BMP-3) (Tyr67Asn), 3) Homeobox protein hox-A2 (HOXA2) (Val327Ile), 4) Rho-GTPase activating protein (ARHGAP 21) (Gly1121Ser), 5) Myosin 1H (MYO1H) (rs10850110).
Authors
- Amol Patil (ORCID: https://orcid.org/0000-0002-8636-4336)
- Monali R. Nikalje (ORCID: https://orcid.org/0000-0003-1258-128X)
- Jayesh Rahalkar (ORCID: https://orcid.org/0000-0002-9192-0413)
- Anand Sabane
- Tulsi Subramaniam (ORCID: https://orcid.org/0000-0002-9150-2502)
- Anish Doke
Institutions
- Symbiosis International University (IN)
- Dr. D.Y. Patil Vidyapeeth, Pune (IN)
- Bharati Vidyapeeth (Deemed to be University) (IN)
Publication Details
- Journal
- Folia Medica
- Published
- 2024-08-31
- DOI
- https://doi.org/10.3897/folmed.66.e129047
- Citations
- 1
- Primary Topic
- Cleft Lip and Palate Research
- Type
- article
- Field-Weighted Citation Impact
- 0.55