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Open AccessDental management of severe dentinogenesis imperfecta in a mild form of osteogenesis imperfecta
Dental management of severe dentinogenesis imperfecta in a mild form of osteogenesis imperfecta
1Faculty of Dentistry, University of the Western Cape, UWC Dental Special Dental Clinic for Genetic Disorders, Red Cross Children's Hospital, Rondebosch, Cape Town
2Department of Human Genetics, University of the Western Cape, UWC Dental Special Dental Clinic for Genetic Disorders, Red Cross Children's Hospital, Rondebosch, Cape Town
DOI: 10.17796/jcpd.26.2.r852g46052604266 Vol.26,Issue 2,April 2002 pp.131-136
Published: 01 April 2002
*Corresponding Author(s): L.X.G. Stephen E-mail: LStephen@uwc.ac.za
Abstract
Dentinogenesis Imperfecta (DI), in which the teeth are discolored, translucent and brittle, can occur in isolation as a familial trait and as a component of the skeletal dysplasia Osteogenesis Imperfecta (OI). In a Cape Town family, 20 persons in 3 generations had mild OI, with the additional manifestation of severe DI. The family was assessed at the Dental Genetic Unit of the University of the Western Cape and appropriate dental treatment was provided. In this setting, a detailed treatment plan was devised for a severely affected woman.This plan proved to be efficient and cost effective, and the final outcome was pleasing to the patient. Dentinogenesis Imperfecta is not uncommon and may well be encountered in conventional dental practice. The necessary clinical expertise is within the scope of the skills of the general dentist.
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L.X.G. Stephen,P. Beighton. Dental management of severe dentinogenesis imperfecta in a mild form of osteogenesis imperfecta. Journal of Clinical Pediatric Dentistry. 2002. 26(2);131-136.
References
1. Tsipouras P. in Beighton P (ed) McKusick’s Heritable Disorders of Connective Tissue. 5th ed. St Louis: Mosby, p. 218-314, 1993.
2. Beighton P, Spranger J, Versfeld G. Skeletal complications in osteogenesis imperfecta, a review of 153 South African patients. S Afr Med J 64: 565-568, 1983.
3. Beighton P, Versfeld GA. On the paradoxically high relative prevalence of osteogenesis imperfecta type III in the black pop-ulation of South Africa. Clin Genet 27: 398-401, 1985.
4. Viljoen D, Beighton P. Osteogenesis imperfecta type III: an ancient mutation in Africa? Am J Med Genet 27: 907-912, 1987.
5. Beighton P. Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta? J Med Genet 18: 124-128, 1981.
6. Levin LS, Brady JM, Melnick M. Scanning electron microscopy of teeth in dominant osteogenesis imperfecta. Am J Med Genet 5: 189-199, 1980.
7. Paterson CR, McAllion S, Miller R. Heterogeneity of osteogene-sis imperfecta type I. J Med Genet 20: 203-205, 1983.
8. Witkop CJ Jr., Rao SR. Inherited defects in tooth structure. Birth Defects Orig Art Ser 7: 153-184, 1971.
9. Shields ED, Bixler D, El-Kafrawy AM. A proposed classification for heritable human dentine defect with a description of a new entity. Arch Oral Biol 18: 543-553, 1973.
10. Witkop CJ Jr. Hereditary defects of dentin. Dent Clin N Am 19: 25-45, 1975.
11. Broughman JA, Halloran SL, Roulston D et al. An autosomal dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc. J Craniofac Genet Dev Biol 6: 341-350, 1986.
12. Dean JA, Hartsfield JK Jr., Wright JT, Hart TC. Dentin dysplasia, type II linkage to chromosome 4q. J Craniofac Genet Dev Biol 17: 172-177, 1997.
13. MacDougall M, Jeffords LG, Gu TT et al. Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q. J Dent Res 78: 1277-1282, 1999.
14. Raff ML, Craigen WJ, Smith LT, Keene DR, Byers PH. Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII. Hum Genet 106: 19-28, 2000.
15. Giansanti JS, Allen JD. Dentin dysplasia, type II, or dentin dys-plasia, coronal type. Oral Surg 38: 911-917, 1974.
16. Wald C, Diner H. Dysplasia of the dental pulp: report of a case. J Dent Child 41: 212-215, 1974.
17. Nayer AK, Latta JB, Soni NN. Treatment of dentinogenesis imper-fecta in a child: report of a case. J Dent Child 48: 453-455, 1981.
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