Abstract

Dental sciences are an area of specialization which involves not only the oral cavity but the adjoining head and neck region. The different specialties of dentistry range from diagnosis to treatment of dental diseases. In a developing country like India, the total population and number of dental institutes account for the second highest number in the world. The role of research is imperative. The area of research in dentistry can range from epidemiology, material sciences and upto genomic research. The focus of molecular studies in dentistry is primarily oriented towards identifying the etiology, pathogenesis and prognosis of various disease processes. The limitations of doing genomic research in a developing country are paucity of funds or the access to the advanced laboratory infrastructure. Genetic studies in dentistry include identification of molecular alterations during embryologic development, microflora in infections and habit associated carcinogenesis. Microbial studies in dentistry are often focused on microflora in dental caries, periapical infection or periodontal pathologies. Recently, studies on the role of Human Papilloma Virus (HPV) in oral squamous cell carcinoma and oral manifestations of HIV viruses have gained more relevance. Syndromes with craniofacial manifestations are common in dental practice and often studied for the underlying genetic defects. Racial variations and associated gene polymorphisms in prevalence of developmental disorders are also evaluated. Genomic changes can be associated with development disorders of tooth or jaw, such as tooth agenesis or structural defects of tooth (Amelogenesis imperfecta & Dentinogenesis imperfecta) and cleft palate affecting the jaws. The tooth formation is controlled by a group of homeobox genes. Amelogenesis imperfecta is often associated with tricho-dento-osseous syndrome, where there is a mutation of homeobox gene known as Dlx (distal less homeobox gene) is associated with tooth development. Tooth agenesis is a clinical manifestation in Witkop’s syndrome which is associated with a nonsense mutation of MSX-1 (Muscle segment homeobox) gene. MSX-1 is also found to be altered in patients with cleft lip & cleft palate [1,2,3].

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.