Multidisciplinary treatment of non-syndromic oligodontia

European Journal of Dentistry

Volumn 6, Issue 2, 2012, Pages 218-226

  Bural, Canan ^a   Oztas, Evren ^a   Ozturk, Sukru ^b   Bayraktar, Gulsen ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Non syndromic autosomal recessive linked oligodontia; Oligodontia; Pre prosthetic orthodontic therapy; Prosthetic therapy; Severe hypodontia

Indexed keywords

EID: 84861163564     PISSN: 13057456     EISSN: 13057464     Source Type: Journal    
DOI: None     Document Type: Article

References (27)

1. Dhanrajani PJ. Hypodontia: etiology, clinical features, and management. Quintessence Int 2002;33:294-302.
2. Gorlin RJ, Cohen M Jr, Leven L, eds. Syndromes of the head and neck. 3rd ed. New York: Oxford University Press, 1990.
3. Polder BJ, Van't Hof MA, Van der Linden FP, Kuijpers-Jagtman AM. A meta-analysis of the prevalence of dental agenesis of permanent teeth. Community Dent Oral Epidemiol 2004;32:217-226.
4. Jepson NJ, Nohl FS, Carter NE, Gillgrass TJ, Meechan JG, Hobson RS, Nunn JH. The interdisciplinary management of hypodontia: restorative dentistry. Br Dent J 2003;194:299-304.
5. Schalk-van der Weide Y, Beemer FA, Faber JA, Bosman F. Symptomatology of patients with oligodontia. J Oral Rehabil 1994;21:247-261.
6. Hall RK. Congenitally missing teeth-a diagnostic feature in many syndromes of the head and neck. Int Ass Dent Child 1983;14:69-75.
7. Schalk-van der Weide Y, Steen WH, Bosman F. Distribution of missing teeth and tooth morphology in patients with oligodontia. ASDC J Dent Child 1992;59:133-140.
8. Dermaut LR, Goeffers KR, De Smit AA. Tooth agenesis correlated with jaw relationship and crowding. Am J Orthod Dentofac Orthop 1986;90:204-210.
9. Kotsiomiti E, Kassa D, Kapari D. Oligodontia and associated characteristics: assessment in view of prosthodontic rehabilitation. Eur J Prosthodont Restor Dent 2007;15:55-60.
10. Bailleul-Forestier I, Berdal A, Vinckier F, de Ravel T, Fryns JP, Verloes A. The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement. Eur J Med Genet 2008;51:383-408.
11. Prabhu NT, John R, Munshi AK. Rieger's syndrome: a case report. Quintessence Int 1997;28:749-752.
12. Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. A nonsense mutation in MSX1 causes Witkop syndrome. Am J Hum Genet 2001;69:67-74.
13. Gurrieri F, Franco B, Toriello H, Neri G. Oral-facial-digital syndromes: review and diagnostic guidelines. Am J Med Genet A 2007;143A:3314-3323.
14. McGovern E, Al-Mudaffer M, McMahon C, Brosnahan D, Fleming P, Reardon W. Oculo-facio-cardio-dental syndrome in a mother and daughter. Int J Oral Maxillofac Surg 2006;35:1060-1062.
15. Minić S, Novotny GE, Trpinac D, Obradović M. Clinical features of incontinentia pigmenti with emphasis on oral and dental abnormalities. Clin Oral Investig 2006;10:343-347.
16. Mostowska A, Kobielak A, Trzeciak WH. Molecular basis of non-syndromic tooth agenesis: Mutations of MSX1 and PAX9 reflect their role in patterning human dentition. Eur J Oral Sci 2003;111:365-370.
17. Mostowska A, Biedziak B, Trzeciak WH. A novel mutation in PAX9 causes familial form of molar oligodontia. Eur J Hum Genet 2006;14:173-179.
18. Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P. A missense mutation in PAX9 in a family with distinct phenotype of oligodontia. European J Hum Genet 2003;11:866-871.
19. Kim JW, Simmer JP, Lin BP, Hu JCC. Novel MSX1 Frameshift causes autosomal-dominant oligodontia. J Dent Res 2006;85:267-271.
20. Pereira TV, Salzano FM, Mostowska A, Trzeciak WH, Ruiz-Linares A, Chies JA, Saavedra C, Nagamachi C, Hurtado AM, Hill K, Castro-de-Guerra D, Silva-Júnior WA, Bortolini MC. Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development. Proc Natl Acad Sci U S A 2006;103:5676-5681.
21. van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet 2000;24:342-343.
22. Imirzalioglu P, Uckan S, Haydar SG. Surgical and prosthodontic treatment alternatives for children and adolescents with ectodermal dysplasia: a clinical report. J Prosthet Dent 2002;88:569-572.
23. Finnema KJ, Raghoebar GM, Meijer HJ, Vissink A. Oral rehabilitation with dental implants in oligodontia patients. Int J Prosthodont 2005;18:203-209.
24. Bani M, Tezkirecioglu AM, Akal N, Tuzuner T. Ectodermal dysplasia with anodontia: a report of two cases. Eur J Dent 2010 Apr;4:215-222.
25. Kinzer GA, Kokich VO Jr. Managing congenitally missing lateral incisors. Part II: tooth-supported restorations. J Esthet Restor Dent 2005;17:76-84.
26. Robertsson S, Mohlin B. The congenitally missing upper lateral incisor. A retrospective study of orthodontic space closure versus restorative treatment. Eur J Orthod 2000;22:697-710.
27. Gross MD, Nissan J, Ormianer Z, Dvori S, Shifman A. The effect of increasing occlusal vertical dimension on face height. Int J Prosthodont 2002;15:353-357.