Non-syndromic agenesis of permanent teeth is one of the most common anomalies in human development, a multifactorial characteristic caused by genetic and environmental factors. We describe a pair of monozygotic twins who showed second premolar and third molar agenesis, albeit with different expressions. We studied the DNA of two genes, paired domain box gene 9 (PAX9) and muscle segment homeodomain-homeobox1 (MSX1), encoding transcription factors that earlier studies found were involved in the manifestation of this condition. No specific causative mutation was found. However, we detected a C→T change in MSX1 exon 2 in both twins, suggesting that this polymorphism might be involved in the trait's expression. © The Authors 2013.
CITATION STYLE
Lopez, S. I. N., Mundstock, K. S., Paixão-Côrtes, V. R., Schüler-Faccini, L., Mundstock, C. A., Bortolini, M. C., & Salzano, F. M. (2013). MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis. Twin Research and Human Genetics, 16(6), 1112–1116. https://doi.org/10.1017/thg.2013.69
Mendeley helps you to discover research relevant for your work.