Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
Staudt, C. B. & Kiliaridis, S. Different skeletal types underlying Class III malocclusion in a random population. Am. J. Orthod. Dentofac. Orthop. 136, 715–721 (2009).
Zere, E., Chaudhari, P. K., Sharan, J., Dhingra, K. & Tiwari, N. Developing Class III malocclusions: challenges and solutions. Clin. Cosmet. Investig. Dent. 10, 99–116 (2018).
Gershater, E. et al. Genes and pathways associated with skeletal sagittal malocclusions: a systematic review. Int. J. Mol. Sci. 22, 13037 (2021).
Dehesa-Santos, A., Iber-Diaz, P. & Iglesias-Linares, A. Genetic factors contributing to skeletal class III malocclusion: a systematic review and meta-analysis. Clin. Oral. Investig. 25, 1587–1612 (2021).
Zohud, O. et al. Towards genetic dissection of skeletal Class III malocclusion: a review of genetic variations underlying the phenotype in humans and future directions. J. Clin. Med. 12, 3212 (2023).
Zhou, X. et al. Genetic architecture of non-syndromic skeletal class III malocclusion. Oral. Dis. 29, 2423–2437 (2023).
Amanat, S., Requena, T. & Lopez-Escamez, J. A. A systematic review of extreme phenotype strategies to search for rare variants in genetic studies of complex disorders. Genes 11, 987 (2020).
Zoghbi, A. W. et al. High-impact rare genetic variants in severe schizophrenia. Proc. Natl Acad. Sci. USA 118, e2112560118 (2021).
Sfondrini, M. F., Gandini, P., Alcozer, R., Vallittu, P. K. & Scribante, A. Failure load and stress analysis of orthodontic miniscrews with different transmucosal collar diameter. J. Mech. Behav. Biomed. Mater. 87, 132–137 (2018).
Ngan, P. & Moon, W. Evolution of Class III treatment in orthodontics. Am. J. Orthod. Dentofac. Orthop. 148, 22–36 (2015).
Author information
Authors and Affiliations
Contributions
M.L.: writing—original draft; A.S.: writing—original draft, writing—review and editing; E.E.: conceptualization, writing—original draft, writing—review and editing, supervision.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Lecca, M., Scribante, A. & Errichiello, E. Commentary on “Craniofacial Syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis”. Pediatr Res 95, 1412–1414 (2024). https://doi.org/10.1038/s41390-024-03036-3
Received:
Accepted:
Published:
Version of record:
Issue date:
DOI: https://doi.org/10.1038/s41390-024-03036-3