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Implant therapy for a patient with osteogenesis imperfecta type I: review of literature with a case report

References : Implant therapy for a patient

author: Shamit S Prabhu,Kevin Fortier,Michael C May,Uday N Reebye | publisher: drg. Andreas Tjandra, Sp. Perio, FISID

References

  1. Sillence DO, Senn A, Danks DM. Genetic heterogeneity in osteogenesis imperfecta. J Med Genet. 1979;16:101–16.
  2. Orioli IM, Castilla EE, Barbosa-Neto JG. The birth prevalence rates for the skeletal dysplasias. J Med Genet. 1986;23:328–32.
  3. Stevenson DA, Carey JC, Byrne JL, Srisukhumbowornchai S, Feldkamp ML. Analysis of skeletal dysplasias in the Utah population. Am J Med Genet A. 2012;158A:1046–54.
  4. Byers PH. Brittle bones-fragile molecules: disorders of collagen gene structure and expression. Trends Genet. 1990;6:293–300.
  5. Sillence DO, Rimoin DL, Danks DM. Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity. Birth Defects Orig Artic Ser. 1979;15:113–29.
  6. Van Dijk F, Sillence D. Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment. Am J Med Genet A. 2014;164:1470–81.
  7. Levin LS, Brady JM, Melnick M. Scanning electron microscopy of teeth in dominant osteogenesis imperfecta. Am J Med Genet. 1980;5:189–99.
  8. Rios D, Vieira AL, Tenuta LM, Machado MA. Osteogenesis imperfecta and dentinogenesis imperfecta: associated disorders. Quintessence Int. 2005;36:695–701.
  9. Bailleul-Forestier I, Berdal A, Vinchier F, de Ravel T, Fryns JP, Verloes A. The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental development. Eur J Med Genet. 2008;51:383–408.
  10. American Academy of Pediatric Dentristy. Guideline on dental management of heritable dental developmental anomalies. Pediatr Dent. 2016;38:302–7.
  11. Land C, Rauch F, Montpetit K, Ruck-Gibis J, Glorieux FH. Effect of intravenous pamidronate therapy on functional abilities and level of ambulation in children with osteogenesis imperfecta. J Pediatr. 2006;148:456–60.
  12. Rauch F, Munns C, Land C, Glorieux FH. Pamidronate in children and adolescents with osteogenesis imperfecta: effect of treatment discontinuation. J Clin Endocrinol Metab. 2016;91:1268–74.
  13. Bishop N, Adami S, Ahmed SF, Anto’n J, Arundel P, Burren CP, Devogelaer J, et al. Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial. Lancet. 2013;382:1424–32.
  14. Marini J, Forlino A, Bächinger H, Bishop N, Byers P, Paepe A, et al. Osteogenesis imperfecta. Nat Rev Dis Primers. 2017;3:17052.
  15. Marx RE, Shellenberger T, Wimsatt J, Correa P. Severely resorbed mandible: predictable reconstruction with soft tissue matrix expansion (tent pole) grafts. J Oral Maxillofac Surg. 2002;60:878–88.
  16. Brånemark PI. Osseointegration and its experimental background. J Prosthet Dent. 1983;50:399–410.
  17. Javed F, Ahmed HB, Crespi R, Romanos GE. Role of primary stability for successful osseointegration of dental implants: factors of influence and evaluation. Interv Med Appl Sci. 2013;5:162–7.
  18. Wanfors K, Johansson C, Donath K. Augmentation of the mandible via a “tent-pole” procedure and implant treatment in a patient with type III osteogenesis imperfecta: clinical and histologic consideration. Int J Oral Maxillofac Implants. 2009;24:1144–8.
  19. Payne M, Postlethwaite K, Smith D, Nohl F. Implant-supported rehabilitation of an edentate patient with osteogenesis imperfecta: a case report. Int J Oral Maxillofac Implants. 2008;23:947–52.
  20. Binger T, Rucker M, Spitzer WJ. Dentofacial rehabilitation by osteodistraction, augmentation and implantation despite osteogenesis imperfecta. Int J Oral Maxillofac Surg. 2006;35:559–62.
  21. Lee C, Ertel S. Bone graft augmentation and dental implant treatment in a patient with osteogenesis imperfecta: review of the literature with a case report. Implant Dent. 2003;12:291–3.
  22. Zola MB. Staged sinus augmentation and implant placement in a patient with osteogenesis imperfecta. J Oral Maxillofac Surg. 2000;58:443–7.
  23. Friberg B. Brånemark system implants and rare disorders: a report of six cases. Int J Periodontics Restorative Dent. 2013;33:139–48.
  24. Prabhu N, Stevenson A, Cameron A. The placement of osseointegrated dental implants in a patient with type IV B osteogenesis imperfecta: a 9-year follow-up. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007;103:349–51.
  25. Jensen JL, Brox HT, Storhaug K, Ambjørnsen E, Støvne SA, Bjørnland T. Dental implants in patients with osteogenesis imperfecta: a retrospective and prospective study with review of the literature. Oral Surg. 2011;4:105–14.
  26. Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, et al. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta. New Eng J Med. 2006;355:2757–64.
  27. Radunovic Z, Wekre LL, Diep LM, Steine K. Cardiovascular abnormalities in adults with osteogenesis imperfecta. Am Heart J. 2011;161:523–9.
  28. Glorieux FH, Rauch F, Plotkin H, Ward L, Travers R, Roughley P, et al. Type V osteogenesis imperfecta: a new form of brittle bone disease. J Bone Miner. 2000;15:1650–8.
  29. Cho TJ, Lee KE, Lee SK, Song SJ, Kim KJ, Jeon D, et al. A single recurrent mutation in the 5-prime UTR of IFITM5 causes osteogenesis imperfecta type V. Am J Hum Genet. 2012;91:343–8.
  30. Glorieux FH, Ward LM, Rauch F, Lalic L, Roughley PJ, Travers R. Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect. J Bone Miner. 2002;17:30–8.
  31. Ward LM, Rauch F, Travers R, Chabot G, Azouz EM, Lalic L, et al. Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease. Bone. 2002;31:12–8.
  32. Cabral WA, Chang W, Barnes AM, Weis M, Scott MA, Leikin S, et al. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta. Nat Genet. 2007;39:359–65.
  33. Van Dijk FS, Nesbitt IM, Zwikstra EH, Nikkels PGJ, Piersma SR, Fratantoni SA, et al. PPIB mutations cause severe osteogenesis imperfecta. Am J Hum Genet. 2009;85:521–7.
  34. Christiansen HE, Schwarze U, Pyott SM, AlSwaid A, Al Balwi M, Alrasheed S, et al. Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86:389–98.
  35. Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, et al. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86:551–9.
  36. Lapunzina P, Aglan M, Temtamy S, Caparros-Martin JA, Valencia M, Leton R, et al. Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta. Am J Hum Genet. 2010;87:110–4.
  37. Martinez-Glez V, Valencia M, Caparros-Martin JA, Aglan M, Temtamy S, Tenorio J, et al. Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Hum Mutat. 2012;33:343–50.
  38. Shaheen R, Alazami AM, Alshammari MJ, Faqeih E, Alhashmi N, Mousa N, et al. Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation. J Med Genet. 2012;49:630–5.
  39. Keupp K, Beleggia F, Kayserili H, Barnes AM, Steiner M, Semler O, et al. Mutations in WNT1 cause different forms of bone fragility. Am J Hum Genet. 2013;92:565–74.
  40. Pyott SM, Tran TT, Leistritz DF, Pepn MG, Mendelsohn NJ, Temme RT, et al. WNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta. Am J Hum Genet. 2013;92:590–7.
  41. Symoens S, Malfait F, D’hondt S, Callewaert B, Dheedene A, Steyaert W, et al. Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans. Orphanet J Rare Dis. 2013;8:154.
  42. Mendoza-Londono R, Fahiminiya S, Majewski J, Care4Rare Canada Consortium, Tetreault M, Nadaf J, et al. Recessive osteogenesis imperfecta caused by missense mutations in SPARC. Am J Hum Genet. 2015;96:979–85.

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Share: Posted 2021-03-16 08:13:00
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