Heredity of orthodontic anomalies
Authors:
Miroslava Švábová 1; Jaroslav Racek 2; Marie Marková 2
Authors‘ workplace:
Ústav biologie a lékařské genetiky 1. LF UK a VFN, Praha
1; Ústav klinické a experimentální stomatologie 1. LF UK a VFN, Praha
2
Published in:
Čas. Lék. čes. 2013; 152: 180-184
Category:
Review Article
Overview
The survey of most common orthodontic anomalies is given in this article. Authors, utilizing literature data, their own research as well as their therapeutic experience, try to elucidate the role of genetics in determination of dental anomalies and malocclusion. They emphasise the fact that genetically determined orthodontic anomalies are not easy to treat. Retention of treatment result could also be a problem. Occurrence of an anomaly in one member of the family should lead to the examination of other members, especially the young ones.
Keywords:
heredity of orthodontic anomalies – heredity of malocclusion
Sources
1. Schulze CH. Anomalien und Missbildungen der menschlischen Zahne. Berlin, Chicago, London, Sao Paulo, Tokio: Quintessenz Verlag GmbH 1987.
2. Marková M, Taichmanová Z. Incidence of orthodontic anomalies in schoolchildren in Prague. Acta Univ Carol Med 1985; 31: 415–433.
3. Larmour CJ, Mossey PA, Thind BS, Forgie AH, Stirrups DR. Hypodontia – a retrospective review of prevalence and etiology. Part I. Quintessence Int. 2005; 36(4): 263–270.
4. Lammi L, Arte S, Somer M, et al. Mutation in AXIN2 Cause Familial Tooth Agenesis and Predispose to Colorectal Cancer. Am J Hum Genet 2004; 74: 1043–1050.
5. Callahan N, Modesto A, Meira R, Seymen F, Patir A, Vieira AR. Axis Inhibition Protein 2 (AXIN2) Polymorphism and Tooth Agenesis. Arch Oral Biol 2009; 54(1): 45–49.
6. Chalothorn LA, Beeman CS, Ebersole JL, et al. Hypodontia as a risk marker for epithelial ovarian cancer: a case controlled study. J Am Dent Assoc 2008; 139(2): 163–169.
7. Dahlberg AA. Inherited congenital absence of six incisors, deciduous and permanent. J Dent Res 1937; 16: 59–62.
8. Suarez BK, Spence MA. The genetics of hypodontia. J Dent Res 1974; 53: 781–785.
9. Sottner L, Marková M, Racek J, Sigmundová S. Příspěvek k dědičnosti hypodoncie. Čs. Stomat. 1976; 76(6): 420–425.
10. Sottner L, Racek J, Švábová-Sládková M. Nové poznatky v etiologii hypodoncie, 1. část. Čs. Stomat. 1996; 96(1): 4–8.
11. Sottner L, Racek J, Švábová-Sládková M. Nové poznatky v etiologii hypodoncie, 2. část. Čs. Stomat. 1996; 96(2): 50–59.
12. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomainmissense mutation causes selective tooth agenesis. Nat Genet 1996; 13: 417–421.
13. Vastardis H. The genetics of human tooth agenesis: new discoveries for understanding dental anomalies. Am J Orthod Dentofacial Orthop 2000; 117: 650–656.
14. Han D, Gong Y, Wu H, et al. Novel EDA mutation resulting in X- linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis. Eur J Med Genet 2008; 51(6): 536–546.
15. Online Mendelian Inheritance in Man. Dostupné na: http://www.ncbi.nlm.nih.gov/omim.
16. Nawaz S, Klar J, Wajid M, et al. WNT10A missense mutation associated with a complete Odonto-Onycho- Dermal Dysplasia syndrome. Eur J Med Genet 2009; 17: 1600–1605.
17. Mostowska A, Biedziak B, Zadurska M, Dunin-Wilczynska I, Lianeri M,Jagodzinski P. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis. Clin Genet 2012, Nov 20. doi: 10.1111/cge. 12061.
18. Hoffmeister H. Mikrosymptome als Hinweis auf vererbte Unterzahl, Uberzahl und Verlangerung von Zahnen. Dtsch zahnarztliche Z 1977; (32): 551–561.
19. Marková M, Vášková J. Nový pohled na problematiku hypodoncie.Čs. Stomat. 1989; 89(6): 416–424.
20. Racek J, Sottner L. Naše názory na dědičnost retence špičáku. Sborn lék. 1984; 86(11–12): 355–360.
21. Peck S, Peck L, Kataja M. Concomitant occurence of canine malposition and tooth agenesis: Evidence of orofacial genetic fields. Am J Orthod 2002; 122(6): 657–668.
22. Pirinen S, Arte S, Apajalahti S. Palatal Displacement of Canine is Genetic and Related to Congenital Absence of Teeth. J Dent Res 1996; 75(10): 1742–1746.
23. Bjerklin K, Kurol J, Valentin J. Ectopic eruption of maxillary first permanent molars and association with other tooth and developmental disturbances. Eur J Orthod 1992; 14: 369–375.
24. Mossey PA. The Heritability of malocclusion: Part 2. The Influence of Genetics in Malocclusion, Br J Orthod 1999; 26(3): 195–203.
25. Manfredi C, Martina R, Grossi GB, Giuliani M. Heritability of 39 orthodontic cephalometric parameters on MZ, DZ twins and MN – paired singletons, Am J Orthod Dentofacial Orthop 1997; 111(1): 44–51.
26. Savoye I, Loos R, Carels C, Derom C, Vlietinck R. A genetic study of anteroposterior and vertical facial proportions using model-fitting, Angle Orthod 1998; 68(5): 467–470.
27. Naini FB, Moss PJ. Three-dimensional assessment of the relative contribution of genetics and environment to various facial parameters with the twin method, Am J Orthod Dentofacial Orthop 2004; 126(6): 655–665.
28. Proffit WR. Contemporary Orthodontics, Fourth Edition. St. Louis: Mosby Elsevier 2007.
29. Normando D, Faber J, Guerreiro JF, Quintao CC. Dental Occlusion in a Split Amazon Indigenous Population: Genetics Prevails over Environment. PLoS ONE 2011; 6(12): e28387.
30. Normando D, Almeida MA, Quintao CC. Dental crowding. Angle Orthod 2013; 83(1): 10–15 doi: 10.2319/02112-91.1. [Epub 2012 Jul 13].
31. Ting TY, Wong RW, Rabie AB. Analysis of genetic polymorphism in skeletal Class I crowding. Am J Orthod Dentofacial Orthop 2011; 140(1): e19–15. doi: 10.1016/j.ajodo.2010.12.015.
32. Racek J. Nové poznatky v epidemiologii ortodontických anomálií a indikace k léčbě. Autoreferát dizertace k získání vědecké hodnosti doktora lékařských věd. Praha: Univerzita Karlova 1989.
33. Racek J, Koťová M, Sottner L. Výskyt anomálií orofaciální orofaciální oblasti u školních dětí pražské a jindřichohradecké populace. Epidemiologická studie. Čs. Stomat. 1979; 79(4): 271–276.
34. Racek J, Koťová M, Sottner L. Výskyt ortodontických anomálií u školních dětí cikánského původu. Čs. Stomat. 1980; 80(4): 254–258.
35. Marková M. Dědičnost ortodontických anomálií prognatního charakteru. Zpráva pro závěrečné oponentní řízení dílčího výzkumného úkolu. Praha: FVL UK 1985.
36. Kawala B, Antoszewska J, Necka A. Genetics or environment? A twin – method study of malocclusions. World J Orthod 2007; 8(4): 405–410.
37. Rabie ABM. Condylar growth: From functional appliance to gene therapy. 85th Congress of the European Orthodontic Society, Helsinki 2009.
38. Franchi L, Baccetti T. Prediction of individual mandibular changes induced by functional jaw orthopedics followed by fixed appliances in Class II patients. Angle Orthod 2006; 76(6): 950–954.
39. Peck S, Peck L, Kataja M. Class II Division 2 malocclusion : a heritable pattern, Angle Orthodontist 1998; 68: 9–17.
40. Alvarez G, Ceballos FC, Quinteiro C. The role of inbreeding in the extinction of a European royal dynasty. PLoS One 2009; 4(4): e5174, Epub 2009 Apr 15.
41. Wolf G, Wienker TF, Sander H. On the genetics of mandibular prognathism: analysis of large European noble families. J Med Genet 1993; 30: 112–116.
42. Cruz RM, Krieger H, Ferreira R, Mah J, Hartsfield J Jr, Oliveira S. Major gene and multifactorial inheritance of mandibular prognathism. Am J Med Genet A 2008; 146 A(1): 71–77.
43. Watanabe M, Suda N, Ohyama K. Mandibular prognathism in Japanese families ascertained through orthognathically treated patients. Am J Orthod Dentofacial Orthop 2005; 128(4): 466–470.
44. Frazier- Bowers S, Rincon-Rodriguez R, Zhou J, Alexander K, Lange E. Evidence of Linkage in Hispanic Cohort with Class III Dentofacial Phenotype. J Dent Res 2009; 88(1): 56–60.
45. Li Q, Zhang F, Li X, Chen F. Genome Scan for Locus Involved in Mandibular Prognathism in Pedigrees from China. PLoS ONE 2010; 5(9): e12678., doi: 10.1371/journal.pone.0012678.
46. Xue F, Wong RWK, Rabie ABM. Genes, genetics, and Class III malocclusion. Orthod Craniofac Res 2010; 13(2): 69–74.
47. Rahimov F, Jugessur A, Murray CJ. Genetics of Nonsyndromic Orofacial Clefts. Cleft Palate Craniofac Journal 2012; 49(1): 73–91.
48. Hennekam RCM, Krantz ID, Allanson JE. Gorlin´s Syndromes of the Head and Neck. Oxford: University Press 2010.
Labels
Addictology Allergology and clinical immunology Angiology Audiology Clinical biochemistry Dermatology & STDs Paediatric gastroenterology Paediatric surgery Paediatric cardiology Paediatric neurology Paediatric ENT Paediatric psychiatry Paediatric rheumatology Diabetology Pharmacy Vascular surgery Pain managementArticle was published in
Journal of Czech Physicians
Most read in this issue
- The clefts as inborn defects
- Heredity of orthodontic anomalies
- Twin studies in stomatology
- Orthodontic anomalies and secular trend in formation of the orofacial cranium