Acessibilidade / Reportar erro

Dentinogenesis imperfecta type II: approach for dental treatment

Dentinogênese imperfeita tipo II: abordagem de tratamento odontológico

Abstracts

INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affects both primary and permanent dentitions. The DI characteristics are discolored and translucent teeth ranging from gray to brownish-blue or amber. The enamel may split readily from the dentin when subjected to occlusal stress. Radiographically there are evident of cervical constrictions, short root and pulp chambers, and the root canals are smaller than normal or completely obliterated. The dental treatment choice can be decided on a case-by case‑basis, considering the degree of dental tissue loss, and child age and cooperation. OBJECTIVE: The aim of this case report was to describe the early dental treatment performed in a child affected by DI type II. CASE REPORT: The treatment involved basic preventive procedures. Primary molars were worn to such an extent that the remained tooth structure was covered with composite resin to protect the exposed dentin. Resin-based sealant was applied in all first permanent molars. Posterior cross bite was treated with the expansion of the upper arch. CONCLUSION: The early treatment restored the patient´s vertical dimension resulting in acceptable esthetics and function for the permanent teeth to complete their eruption.

Dentinogenesis imperfecta; tooth anomaly; dental care


INTRODUÇÃO: A dentinogênese imperfeita (DI) é uma desordem hereditária no desenvolvimento da dentina, que afeta tanto a dentição decídua quanto a permanente. A DI apresenta como características dentes escurecidos e translúcidos que vão do cinza ao marrom ou âmbar. O esmalte pode se separar facilmente da dentina quando submetido ao estresse oclusal. Radiograficamente há evidencias de constrição cervical, raiz curta e polpas reduzidas, sendo os canais menores do que o comum ou completamente obliterados. A escolha do tratamento pode ser decidida com base no caso, considerando-se a idade da criança, grau de perda de tecido dentário e de cooperação do paciente. OBJETIVO: O objetivo deste relato de caso foi descrever o tratamento odontológico precoce realizado em uma criança afetada pela DI tipo II. RELATO DO CASO: O tratamento envolveu procedimentos básicos de prevenção. Molares decíduos foram desgastados, de tal forma que a estrutura remanescente do dente foi coberta com resina composta para proteger a dentina exposta. Selante resinoso foi aplicado em todos os primeiros molares permanentes. Mordida cruzada posterior foi tratada com a expansão do arco superior. CONCLUSÃO: O tratamento precoce restaurou a dimensão vertical do paciente resultando em estética e função aceitáveis para os dentes permanentes completarem sua erupção.

Dentinogênese imperfeita; anormalidades dentárias; assistência odontológica


  • 1
    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. 2011;17:314-9. PMid:21029264. http://dx.doi.org/10.1111/j.1601-0825.2010.01760.x
  • 2
    Shields E, Bixler D, El-Kafrawy A. A proposed classification for heritable human dentin defects with a description of a new entity. Arch Oral Biol. 1973;18:543-53. http://dx.doi.org/10.1016/0003-9969(73)90075-7
  • 3
    MacDougall M. Dental structural diseases mapping to human chromosome 4q21. Connect Tissue Res. 2003;44:285-91. PMid:12952210.
  • 4
    Witkop CJ Jr. Hereditary defects in enamel and dentin. Acta Genet. 1957;7:236-9. PMid:13469154.
  • 5
    Skillen WG. Histologic and clinical study of hereditary opalescent dentin. J Am Dent Assoc. 1937;24:1426-33.
  • 6
    Roberts DW, Woolridge ED. A case of Dentinogenesis Imperfecta. A six month evaluation. N Y State Dent J. 1977;43:286-9. PMid:266142.
  • 7
    Mayordomo FG, Estrela F, de Aldecoa EA. Dentinogenesis Imperfecta: a case report. Quintessence Int. 1992;23:795-802. PMid:1305296.
  • 8
    Talbot ES. Arrests of development and descalcification of the enamel and dentine. J Am Med Assoc. 1893;20:29-32. http://dx.doi.org/10.1001/jama.1893.02420290003001a
  • 9
    Roberts E, Schour I. Hereditary opalescent dentine (dentinogenesis imperfecta). Am J Orthod Oral Surg. 1939;25:267-76. http://dx.doi.org/10.1016/S0096-6347(39)90098-0
  • 10
    McKusick VA. OMIM (Online Mendelian Inheritance In Man) [cited 2012 May 18]. Available from: http://www.ncbi.nlm.nih.gov/omim/
  • 11
    Gallusi G, Libonati A, Campanella V. SEM-morphology in dentinogenesis imperfecta type II: microscopic anatomy and efficacy of a dentine bonding system. Eur J Paediatr Dent. 2006;7:9-17. PMid:16646639.
  • 12
    Baldini V, Tagliaferro EP, Ambrosano GM, Meneghim Mde C, Pereira AC. Use of occlusal sealant in a community program and caries incidence in high-and-low-risk children. J Appl Oral Sci. 2011;19:396-402. PMid:21710092. http://dx.doi.org/10.1590/S1678-77572011005000016
  • 13
    MacDougall M, DuPont B, Simmons D, Reus B, Krebsbach P, Karrman C, et al. Ameloblantin gene (AMBN) maps within the critical region for autossomal dominant amelogenesis imperfeta at chromosome 4q21. Genomics. 1997;41:115-8. PMid:9126491. http://dx.doi.org/10.1006/geno.1997.4643
  • 14
    Yamakoshi Y, Hu JC, Fukae M, Zhang H, Simmer JP. Dentin glycoprotein: the protein in the middle of the dentin sialophosphoprotein chimera. J Biol Chem. 2005;280:17472-9. PMid:15728577. http://dx.doi.org/10.1074/jbc.M413220200
  • 15
    Zhang X, Zhao J, Li C, Gao S, Qiu C, Liu P, et al. DSPP mutation in dentinogenesis impesfecta Shields type II. Nat Genet. 2001;27:151-2. PMid:11175779. http://dx.doi.org/10.1038/84765
  • 16
    Xiao S, Yu C, Chou X, Yuan W, Wang Y, Bu L, et al. Dentinogenesis imperfecta 1 with or wiyhout progressive hering loss is associated with distinct mutations in DSPP. Nat Genet. 2001;27:201-4. PMid:11175790. http://dx.doi.org/10.1038/84848
  • 17
    Malmgren B, Lindskog S, Elgadi A, Norgren S. Clinical, histopathologic, and genetic investigation in two large families with dentinogeneseis imperfecta type II. Hum Genet. 2004;114:491-8. PMid:14758537. http://dx.doi.org/10.1007/s00439-004-1084-z
  • 18
    Kim JW, Hu JC, Lee JI, Moon SK, Kim YJ, Jang KT, et al. Mutation hot spot in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet. 2005;116:186-91. PMid:15592686. http://dx.doi.org/10.1007/s00439-004-1223-6
  • 19
    Witkop CJ Jr. Hereditary defects of dentin. Dent Clin North Am. 1975;19:25-45. PMid:162890.
  • 20
    Wang H, Hou Y, Cui Y, Huang Y, Shi Y, Xia X, et al. A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenisis imperfecta type II. Mutat Res. 2009;662:22-7. PMid:19103209. http://dx.doi.org/10.1016/j.mrfmmm.2008.11.019
  • 21
    Song Y, Wang C, Peng B, Ye X, Zhao G, Fan M, et al. Phenotypes and genotypes in 2 DGI families with different DSPP mutations. Oral Surg Oral Med Oral Pathol Oral Radiol Endond. 2006;102:360-74. PMid:16920545. http://dx.doi.org/10.1016/j.tripleo.2005.06.020
  • 22
    Holappa H, Nieminen P, Tolva L, Lukinmaa PL, Alaluusua S. Splicing site mutations in dentin sialophosphoprotein causing dentinogenisis imperfecta tipe II. Eur J Oral Sci. 2006;114:381-4. PMid:17026502. http://dx.doi.org/10.1111/j.1600-0722.2006.00391.x
  • 23
    Kida M, Tsutsumi T, Shindoh M, Ikeda H, Ariga T. De novo mutation in the DSPP gene associated with dentinogenisis imperfecta type II in a Japanese family. Eur J Oral Sci. 2009;117:392-9. PMid:20121932. http://dx.doi.org/10.1111/j.1600-0722.2009.00683.x
  • 24
    Lee SK, Lee KE, Jeon D, Lee G, Lee H, Shin CU, et al. A novel mutation in the DSPP gene associated with dentinogenisis imperfecta type II. J Dent Res. 2009;88:51-5. PMid:19131317. http://dx.doi.org/10.1177/0022034508328168
  • 25
    Nieminen P, Papagiannoulis-Lascarides L, Waltimo-Siren J, Ollila P, Karjalainen S, Arte S, et al. Frameshift mutations in dentin phosphoproteinand dependence of dentin disease phenotype on mutation location. J Bone Miner Res. 2011;26:873-80. PMid:20949630. http://dx.doi.org/10.1002/jbmr.276
  • 26
    Bixler D. Genetic aspects of dental anomalies. In: McDonald RE, Avery DR. Dentistry for the child and adolescent. 6th ed. St Louis: CV Mosby Co; 1994.

Publication Dates

  • Publication in this collection
    06 Feb 2013
  • Date of issue
    Dec 2012

History

  • Received
    22 Jan 2012
  • Accepted
    16 July 2012
Universidade Estadual Paulista Júlio de Mesquita Filho Rua Humaitá, 1680 - Caixa Postal 331, 14801-903 Araraquara,São Paulo,SP, Tel.: (55 16) 3301-6376, Fax: (55 16) 3301-6433 - Araraquara - SP - Brazil
E-mail: adriana@foar.unesp.br