Third molar agenesis in Down syndrome

Acta Odontologica Scandinavica

Volumn 60, Issue 3, 2002, Pages 151-154

  Lomholt, Jens Fog ^b   Russell, Björn G ^b   Stoltze, Kaj ^b   Kjær, Inger ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b NONE

Author keywords

Genetics; Odontogenesis; Tooth agenesis; Trisomy

Indexed keywords

CHI SQUARE DISTRIBUTION; COMPARATIVE STUDY; COMPLICATION; DENMARK; DOWN SYNDROME; FEMALE; GENETICS; GENOTYPE; HUMAN; HYPODONTIA; MALE; MANDIBLE; MAXILLA; MOLAR TOOTH; PANORAMIC RADIOGRAPHY; PHENOTYPE; RADIOGRAPHY; SEX DIFFERENCE; STATISTICS; TOOTH DEVELOPMENT; ARTICLE; CONGENITAL MALFORMATION;

ANODONTIA; CHI-SQUARE DISTRIBUTION; DENMARK; DOWN SYNDROME; FEMALE; GENOTYPE; HUMANS; MALE; MANDIBLE; MAXILLA; MOLAR, THIRD; ODONTOGENESIS; PHENOTYPE; RADIOGRAPHY, PANORAMIC; SEX FACTORS; STATISTICS AS TOPIC; STATISTICS;

EID: 0036614912     PISSN: 00016357     EISSN: None     Source Type: Journal    
DOI: 10.1080/000163502753740160     Document Type: Article

References (39)

1. Peltola JS, Wolf J, Männik A, Russak S, Seedre T, Sirkel M, et al. Radiographic findings in the teeth of 14- to 17-year-old Estonian Schoolchildren in Tartu and Tallin. Acta Odontol Scand 1997; 55:31-5.
2. Clayton JM. Congenital dental anomalies occurring in 3,557 children. ASDC J Dent Child 1956;23:206-8.
3. Lavelle CL, Ashton EH, Flinn RM. Cusp pattern, tooth size and third molar agenesis in the human mandibular dentition. Arch Oral Biol 1970;15:227-37.
4. Garn SM, Lewis AB, Kerewsky RS. Third molar agenesis and size reduction of the remaining teeth. Nature 1963;200:488-9.
5. Bredy E, Erbing C, Hübenthal B. Häufigkeit der Zahnunterzahl bei Anlage und Nichtanlage von Weisheitzähnen. Dtsch Zahn-Mund-Kieferheilkd 1991;79:357-63.
6. Scherngell R. Prävalenz der Nichtanlage und Verlagerung der 3. Molaren bei 9-14 jährigen. Wien Klin Wochenschr 1992;104: 105-6.
7. Davies PL. Agenesis of teeth of the permanent dentition: a frequency study in Sydney schoolchildren. Aust Dent J 1968;13: 146-50.
8. Grahnén H. Hypodontia in the permanent dentition: a clinical and genetical investigation. Odont Revy 1956;7:1-100.
9. Muller TP, Hill IN, Peterson AC, Blayney JR. A survey of congenitally missing permanent teeth. J Am Dent Assoc 1970; 81:101-7.
10. Glenn FB. Incidence of congenitally missing permanent teeth in a private pedodontic practice. ASDC J Dent Child 1961;28:317-20.
11. Baum BJ, Cohen MM. Studies on agenesis in the permanent dentition. Am J Phys Anthropol 1971;35:125-8.
12. Hundstadbraaten K. Hypodontia in the permanent dentition. ASDC J Dent Child 1973;40:31-3.
13. Brown RV. The pattern and frequency of congenital absence of teeth. 1955 Thesis, State University, Iowa.
14. Gimnes HT. En frekvensundersekelse over hypodonti hos skolebørn i Oslo, med særlig henblikk på forekomst av bilateral hypodonti av 2. premolar i underkjeven. Norske Tannlaegeforen Tid 1963;73:141-8.
15. Rølling SG. Hypodontia of permanent teeth in Danish schoolchildren. Scand J Dent Res 1980;88:365-9.
16. Thomsen S. Missing teeth with special reference to population of Tristan de Cunha. Am J Phys Anthropol 1952;10:155-67.
17. Huskins CI. On the inheritance of an anomaly of human dentition. J Hered 1930;21:279-82.
18. Alvesalo L. The influence of sex-chromosome genes on tooth size in man: a genetic and quantitative study. Am J Orthod 1971;60: 420.
19. Jorgenson RJ. Clinician's view of hypodontia. J Am Dent Assoc 1980;101:283-6.
20. Data base: Online Mendelian Inheritance in Man: http:// wvvw.ncbi.nlm.nih.gov/OMIM.
21. Lurie IW, Ilyina HG, Podleschuk LV, Gorelik LB, Zaletajev DV. Chromosome 7 abnormalities in parents of children with holoprosencephaly and hydronephrosis. Am J Med Genet 1990; 35:286-8.
22. Kurisu K, Tabata MJ. Human genes for dental anomalies. Oral Dis 1997;3:223-8.
23. Russell BG, Kjaer I. Tooth agenesis in Down Syndrome. Am J Med Gent 1995; 55:466-71.
24. Shapira J, Chaushu S, Becker A. Prevalence of tooth transposition, third molar agenesis and maxillary canine impaction in individuals with Down syndrome. Angle Orthod 2000;70:290-6.
25. Jensen GM, Cleall JF, Yip ASG. Dentoalveolar morphology and developmental changes in Down's syndrome (trisomi 21). Am J Orthod 1972;64:607-18.
26. Thompson GW, Popovich F, Anderson DL. Third molar agenesis in the Burlington Growth Centre in Toronto. Community Dent Oral Epidemiol 1974;2:187-92.
27. Byron W, Brown Jr, Hollander N. Statistics, a biomedical introduction. New York: John Wiley, 1977.
28. Garn SM, Lewis AB, Bonné B. Third molar formation and its developement course. Angle Othod 1962;32:270-9.
29. Penrose CS. Biology of mental defect. London: Sidwick & Jackson Ltd; 1963.
30. Garn SM, Lewis AB, Vicinus JH. Third molar polymorphism and its significance to dental genetics. J Dent Res 1963;42:1344-63.
31. Kisling E. Cranial morphology in Down's syndrome [Thesis]. Copenhagen: Munksgaard; 1966.
32. Kjær I, Gabór K, Nodal M, Christensen LR. Aetiological aspects of mandibular tooth agenesis - focusing on the role of the nerve, oral mucosa, and supporting tissues. Eur J Orthod 1994;16:371-5.
33. WWW Database. http://bke-it.helsinki.fi. Developmental Biology Programme of the University of Helsinki; 1966.
34. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nature Genet 1996;13:417-21.
35. Goldenberg M, Das P, Messersmith M, Stockton DW, Patel PI, D'Souza RN. Clinical, radiographic and genetic evaluation of a novel form of autosomal-dominant oligodontia. J Dent Res 2000;79:1469-75.
36. Stockton DW, Das P, Goldenberg M, D'Souza RN, Patel PI. Mutation of PAX9 is associated with oligodontia. Nat Genet 2000;24:18-9.
37. Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, et al. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia. EurJ Hum Genet 2001;9:743-6.
38. Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, et al. Suspectible chiasmate configurations of chromosome 21 predispose to nondisjunction in both maternal meiosis I and meiosis II. Nat Genet 1996;14:400-5.
39. Delarbar JM, Theophile D, Rahmnai Z, Chettouh Z, Blouin JL, Prieur M, et al. Molecular mapping of twenty-four features of Down syndrome or chromosome 21. Eur J Hum Genet 1993;1: 114-24.