medigraphic.com
ISSN 1561-297X (Print)

2015, Number 3

<< Back Next >>

Rev Cubana Estomatol 2015; 52 (3)

Alternative treatment for dentinogenesis imperfecta

Montero CME, Casals GY, Valdés BL

Language: Spanish
References: 19
Page: 105-111
PDF size: 294.91 Kb.


ABSTRACT

Dentinogenesis imperfecta is an inherited dominant autosomal condition originating during the histodifferentiation stage of odontogenesis. It is a form of localized mesodermal dysplasia characterized by an alteration in dentin proteins. The purpose of the study was to present an alternative treatment for dentinogenesis imperfecta in children, using stainless steel crowns and adhesive composite resins. A case is presented of an eight-year-old girl attending consultation for pain when eating cold or sweet food, changes in the color and shape of teeth, and psychological disorders related to her personal appearance. No history of the disease was found in the family. Clinical and radiographic examination revealed alterations in the shape and color of teeth as well as the loss of dental tissue, particularly in the first permanent molars, with a reduction in the vertical dimension. Radiographic examination confirmed the presence of permanent successor follicles as well as normal bone structures. Dentinogenesis imperfecta was diagnosed. Stainless steel crowns were placed over the first permanent molars and the second temporary molars with the purpose of restoring the vertical dimension and eliminating the discomfort when eating. Anterior teeth were then restored with adhesive composite resins. Early diagnosis and treatment of this condition is crucial to prevent large tissue destruction. As is shown in the study, treatment in children should consist in placing stainless steel crowns and restoring the teeth with adhesive composite resins until adult age, when other definitive restorations may be performed.


REFERENCES

  1. Barron MJ, McDonnell ST, MacKie I, Dixon MJ. Hereditary dentine disorders: dentinogenesis imperfecta and dentine displasia. Orphanet Journal of Rare Diseases. [En línea]. 2008 [Consultado 29 enero 2013];3:3. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0722.2006.00391.x

  2. Lee SK, Lee KE, Hawang YH, Kida M, Tsutsumi T, Ariga T, et al. Identification of the DPP mutation in a new kindred and phenotype-genotype correlation. Oral Dis. [En línea]. 2011 [Consultado 27 enero 2013];17:314-9. Disponible en: http://dx.doi.org/10.1111/j.1601-0825.2010.01760.x

  3. Scarel-Caminaga R, Cavalcante L, Finoti L, dos Santos MC, Konishi MF, dos Santos-Pinto LA. Dentinogenesis imperfecta type II: approach for dental treatment. Rev Odontol UNESP. [En línea]. 2012 nov-dec [Consultado 7 febrero 2013];41(6):433-7. Disponible en: http://www.hostcentral.com.br/rou/PDF/v41n6a11.pdf

  4. Cobourne M, Sharpe P. Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition. WIREs Dev Biol. [En línea]. 2012. [Consultado 27 enero 2013]. Disponible en: http://wires.wiley.com/WileyCDA/WiresArticle/articles.html?doi=10.1002%2Fwdev.66

  5. Roberts E, Shour I. Hereditary opalescent dentin. Am J Orthod. [En línea]. 1939 [Consultado 29 Enero 2013];25:267-76. Disponible en: http://dx.doi.org/10.1016/j.bbr.2011.03.031

  6. Torres Molina A. Huesos de cristal. Presentación de un caso. MediSur. [En línea]. 2010 [Consultado 25 Enero 2013];8(4):72-4. Disponible en: http://redalyc.uaemex.mx/src/inicio/ArtPdfRed.jsp?iCve=180016115011

  7. Majorana A, Bardellini E, Brunelli PC, Lacaita M, Cazzolla AP, Favia G. Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study. International Journal of Paediatric Dentistry. [En línea]. March 2010 [Consultado 25 Enero 2013];20(2):112–8. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-263X.2010.01033.x/abstract?

  8. American Academy on Pediatric Dentistry Council on Clinical Affairs. Guideline on oral health care/dental management of heritable dental development anomalies. Pediatr Dent. [En línea]. 2008-2009 [Consultado 21 enero 2013];30:196-201. Disponible en: http://www.aapd.org/media/policies.asp

  9. Lee SK, Lee KE, Song S, Hyun H, Lee SH, Kim J. A DSPP mutation causing dentinogenesis imperfecta and characterization of the mutational effect. Biomed Research International [En linea]. 2013 [Consultado 23 enero 2013];Special Issue. Article ID. 948 181, 7 pages. Disponible en: http://dx,doi.org./10.1155/2013/948181

  10. Zhang J, Wang J, Ma Y, Du W, Zhao S, Zhang Z et al. A Novel Splicing Mutation Alters DSPP Transcription and Leads to Dentinogenesis Imperfecta Type II. PLoS ONE. [En linea]. 2011 nov [Consultado 29 enero 2013]; 6(11):e27982. Disponible en: http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0027982

  11. von Marschall, Z, Mok S, Phillips MD, McKnight DA, Fisher LW. Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP. J Bone Miner Res. [En linea]. 2012 [Consultado 24 enero 2013];27:1309-21. Disponible en: http://onlinelibrary.wiley.com/doi/10.1002/jbmr.1573/abstract?deniedAccessCustomisedMes sage=&userIsAuthenticated=false

  12. Rabassa J, Palma C, González Y. Dentinogénesis imperfecta: a propósito de un caso. Odontol Pediatr [En línea]. 2011 Jul/Dic [Consultado 27 enero 2013];10(2):122-30. Disponible en: http://revistas.concytec.gob.pe/scielo.php?script=sci_arttext&pid=S1814-487X2011000200007&lng=es&nrm=iso>. ISSN 1814-487X

  13. Lee KE, Kang HY, Lee SK, Yoo SH, Lee JC, Hwang YH, et al. Novel dentin phosphoprotein mutations in dentinogenesis imperfecta type II. Clinical Genetics. [En línea]. 2011 April [Consultado 25 enero 2013];79(4):378–84. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1399-0004.2010.01483.x/

  14. von Marschall Z, Mok S, Phillips MD, McKnight DA, Fisher LW. Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP. J Bone Miner Res. [En línea]. 2012 [Consultado 24 Enero 2013];27:1309-21. Disponible en: http://onlinelibrary.wiley.com/doi/10.1002/jbmr.1573/abstract?deniedAccessCustomisedMes sage=&userIsAuthenticated=false

  15. Shields ED, Bixler D, el-Kafrawy AM. A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol. 1973;18:543-53.

  16. Kim JW, Hu JC, Lee JI, Moon SK, Kim YJ, Jang KT, et al. Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II. Human Genetics [En línea]. 2005 Feb [Consultado 30 Enero 2013];116(3):186-91. Disponible en: http://link.springer.com/article/10.1007%2Fs00439-004-1223-6?LI=true

  17. Holappa H, Nieminen P, Tolva L, Lukinmaa PL, Alaluusua S. Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II. European Journal of Oral Sciences. [En línea]. 2006 [Consultado 30 enero 2013];114:381–4. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0722.2006.00391.x/

  18. Bencharit S, Byrd WC, Mack CR, Border MB, Wright JT. Full mouth rehabilitation for a patient with dentinogenesis imperfecta: A clinical report. Journal of Oral Implantology [En línea]. Wright 2013. (In-Press). [Consultado 25 Enero 2013]. Disponible en: http://www.joionline.org/doi/abs/10.1563/AAID-JOI-D-12-00217

  19. Bellet LI, Sanclemente C, Casanovas M. Coronas en odontopediatría : Revisión bibliográfica. Dentum. [En línea]. 2006;6(3):11-117. [Consultado 29 enero 2013]. Disponible en: http://www.nexusediciones.com/pdf/de2006_3/den-3-2006-005.pdf




2020     |     www.medigraphic.com