Literature DB >> 20932402

Case report: Rehabilitation of a child with dentinogenesis imperfecta and congenitally missing lateral incisors.

C Millet1, S Viennot, J P Duprez.   

Abstract

BACKGROUND: Dentinogenesis imperfecta is one of the most common hereditary disorders of dentine formation. Opalescent teeth composed of irregularly formed and undemineralised dentine that obliterates pulp chambers and root canals characterize it. Complete-coverage crowns are usually the preferred restoration for patients with this condition. CASE REPORT: A 9 year-old girl presented with dentinogenesis imperfecta, congenitally missing maxillary lateral incisors and maxillary right permanent second molar retention. TREATMENT: The treatment comprised an initial approach to allow the correct eruption of the retained second molar. The use of low-fusion metal ceramic restorations comprised a second stage to improve the aesthetic appearance and decrease the risk of overload on teeth with limited value. FOLLOW-UP: The patient has been recalled regularly and at the last visit, 10 years after initial prosthetic treatment, no problems or signs of complications have occurred. The patient is now aged 25 years and is still satisfied with the prosthetic rehabilitation.
CONCLUSION: This case illustrates the need for appropriate and timely restorative treatment to prevent deterioration of the dentition. This case will also demonstrate that low-fusion metal ceramic restoration is a viable esthetic treatment option for today's patients.

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Year:  2010        PMID: 20932402     DOI: 10.1007/bf03262758

Source DB:  PubMed          Journal:  Eur Arch Paediatr Dent        ISSN: 1818-6300


  30 in total

Review 1.  Dentinogenesis imperfecta-associated syndromes.

Authors:  P N Kantaputra
Journal:  Am J Med Genet       Date:  2001-11-15

2.  Fracture of porcelain-veneered structures in fatigue.

Authors:  B Kim; Y Zhang; M Pines; V P Thompson
Journal:  J Dent Res       Date:  2007-02       Impact factor: 6.116

3.  A proposed classification for heritable human dentine defects with a description of a new entity.

Authors:  E D Shields; D Bixler; A M el-Kafrawy
Journal:  Arch Oral Biol       Date:  1973-04       Impact factor: 2.633

Review 4.  Heritable dentin defects: nosology, pathology, and treatment.

Authors:  H Ranta; P L Lukinmaa; J Waltimo
Journal:  Am J Med Genet       Date:  1993-01-15

5.  An in vitro investigation of the wear of enamel on porcelain and gold in saliva.

Authors:  C H Hacker; W C Wagner; M E Razzoog
Journal:  J Prosthet Dent       Date:  1996-01       Impact factor: 3.426

Review 6.  Hereditary dentin defects.

Authors:  J-W Kim; J P Simmer
Journal:  J Dent Res       Date:  2007-05       Impact factor: 6.116

7.  Orthodontic and orthognathic management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta: a case report.

Authors:  J Kindelan; M Tobin; D Roberts-Harry; R A Loukota
Journal:  J Orthod       Date:  2003-12

8.  Hereditary dentinogenesis imperfecta: a treatment program using an overdenture.

Authors:  A Darendeliler-Kaba; S C Maréchaux
Journal:  ASDC J Dent Child       Date:  1992 Jul-Aug

9.  Diagnostic features and pedodontic-orthodontic management in dentinogenesis imperfecta type II: a case report.

Authors:  K Ch Huth; E Paschos; T Sagner; R Hickel
Journal:  Int J Paediatr Dent       Date:  2002-09       Impact factor: 3.455

Review 10.  Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.

Authors:  Martin J Barron; Sinead T McDonnell; Iain Mackie; Michael J Dixon
Journal:  Orphanet J Rare Dis       Date:  2008-11-20       Impact factor: 4.123

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