An epidemiological study of dental agenesis in a primary health area in Spain: Estimated prevalence and associated factors

Medicina Oral, Patologia Oral y Cirugia Bucal

Volumn 15, Issue 4, 2010, Pages

  Tallón Walton, Victòria ^a   Nieminen, Pekka ^b,c   Arte, Sirpa ^b,c   Carvalho Lobato, Patricia ^a   Ustrell Torrent, Josep Ma ^a   Manzanares Céspedes, Ma Cristina ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b UNIVERSITY OF HELSINKI   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

Craniofacial development; Hypodontia; Prevalence; Tooth abnormalities

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; DISEASE ASSOCIATION; FEMALE; GENETICS; HUMAN; HYPODONTIA; MAJOR CLINICAL STUDY; MALE; MEDICAL LITERATURE; MEDICAL RECORD; MOLAR TOOTH; MOUTH DISEASE; OLIGODONTIA; PHENOTYPE; PRESCHOOL CHILD; PRIMARY HEALTH CARE; SCHOOL CHILD; SPAIN; TOOTH MALFORMATION;

ANODONTIA; CATCHMENT AREA (HEALTH); FEMALE; HUMANS; MALE; PREVALENCE; PRIMARY HEALTH CARE; RISK FACTORS; SPAIN;

EID: 77954587865     PISSN: 16984447     EISSN: 16986946     Source Type: Journal    
DOI: 10.4317/medoral.15.e569     Document Type: Article

References (22)

1. Haavikko K. Hypodontia of permanent teeth. An orthopantomographic study. Suom Hammaslaak Toim. 1971;67:219-25.
2. Brook AH. Dental anomalies of number, form and size: their prevalence in British schoolchildren. J Int Assoc Dent Child. 1974;5:37-53.
3. Aasheim B, Ogaard B. Hypodontia in 9-year-old Norwegians related to need of orthodontic treatment. Scand J Dent Res. 1993;101:25
4. Muller TP, Hill IN, Peterson AC, Blayney JR. A survey of congenitally missing permanent teeth. J Am Dent Assoc. 1970;81:101-7.
5. Peters H, Neubüser A, Kratochwil K, Balling R. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit cranio-facial and limb abnormalities. Genes Dev. 1998;12:2735-47.
6. Hu G, Vastardis H, Bendall AJ, Wang Z, Logan M, Zhang H, et al. Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis. Mol Cell Biol. 1998;18:6044-51.
7. Tallón-Walton V, Manzanares-Céspedes MC, Arte S, Carvalho-Lobato P, Valdivia-Gandur I, Garcia-Susperregui A, et al. Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies. Eur J Oral Sci. 2007;115:427-32.
8. Lammi L, Arte S, Somer M, Jarvinen H, Lahermo P, Thesleff I, et al. Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am J Hum Genet. 2004;74:1043-50.
9. Arte S, Nieminen P, Apajalahti S, Haavikko K, Thesleff I, Pirinen S. Characteristics of incisor-premolar hypodontia in families. J Dent Res. 2001;80:1445-50.
10. Daugaard-Jensen J, Nodal M, Kjaer I. Pattern of agenesis in the primary dentition: a radiographic study of 193 cases. Int J Paediatr Dent. 1997;7:3-7. (Pubitemid 127488499)
11. Pirinen S, Arte S, Apajalahti S. Palatal displacement of canine is genetic and related to congenital absence of teeth. J Dent Res. 1996;75:1742-6.
12. Baccetti T. A controlled study of associated dental anomalies. Angle Orthod. 1998;68:267-74.
13. Apajalahti S, Arte S, Pirinen S. Short root anomaly in families and its association with other dental anomalies. Eur J Oral Sci. 1999;107:97-101.
14. Darwazeh AM, Hamasha AA, Pillai K. Prevalence of taurodontism in Jordanian dental patients. Dentomaxillofac Radiol. 1998;27:163-5.
15. Schalk-van der Weide Y, Steen WH, Bosman F. Taurodontism and length of teeth in patients with oligodontia. J Oral Rehabil. 1993;20:401-12.
16. MacDonald-Jankowski DS, Li TT. Taurodontism in a young adult Chinese population. Dentomaxillofac Radiol. 1993;22:140-4.
17. Roberts-Harry D, Sandy J. Orthodontics. Part 10: Impacted teeth. Br Dent J. 2004;196:319-27.
18. Leco Berrocal MI, Martín Morales JF, Martínez González JM. An observational study of the frequency of supernumerary teeth in a population of 2000 patients. Med Oral Patol Oral Cir Bucal. 2007;12:E134-8.
19. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet. 1996;13:417-21.
20. Stockton DW, Das P, Goldenberg M, D'Souza RN, Patel PI. Mutation of PAX9 is associated with oligodontia. Nat Genet. 2000;24:18-9.
21. Castell C, Tresserras R, Serra J, Goday A, Lloveras G, Salleras L. Prevalence of diabetes in Catalonia (Spain): an oral glucose tolerance test-based population study. Diabetes Res Clin Pract. 1999;43:33-40. (Pubitemid 29096409)
22. Balli MP, Balli ME, Mengoli M, Balli C, Balli F. [Growth, skeletal and dental age in chronic diarrhea in childhood]. Pediatr Med Chir. 1988;10:277-82.