Literature DB >> 21108924

Case report: Clinical, histological and ultrastructural characterization of type II dentinogenesis imperfecta.

C T Leal1, L D Martins, F D Verli, M A L de Souza, M L Ramos-Jorge.   

Abstract

BACKGROUND: Type II dentinogenesis imperfecta (DGIII) is an autosomal dominant dental development anomaly that affects both the primary and permanent dentition. CASE REPORT: This case report describes the clinical, radiographic and morphological characteristics of the teeth of a seven-year-old child with DGI-II determined by optical microscopy and scanning electron microscopy. TREATMENT: This consisted of extraction of the primary teeth with periapical lesions due to the advanced state of tooth resorption. Aesthetic restorations were performed on the mandibular anterior teeth and occlusal fissure sealants were applied to erupting teeth. A removable partial upper denture was made in order to return anterior aesthetic function and to aid mastication and speech. FOLLOW UP: The child was examined at 3 month intervals. Over the following 3 years the prosthesis was replaced due to facial growth and fluoride was applied at each follow-up visit to all teeth. The patient remains in follow up and management.
CONCLUSION: Individuals with DGI-II must not neglect their dental health. Early diagnosis, professional advice and treatment with periodic follow-up can help improve the quality of life of such patients.

Entities:  

Mesh:

Year:  2010        PMID: 21108924     DOI: 10.1007/BF03262769

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


  18 in total

Review 1.  Dentinogenesis imperfecta-associated syndromes.

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

Review 2.  Dentinogenesis imperfecta type II: case report.

Authors:  A Modesto; A C Alves; A R Vieira; W Portella
Journal:  Braz Dent J       Date:  1996

3.  Dentinogenesis imperfecta: endodontic implications. Case report.

Authors:  M T Pettiette; J T Wright; M Trope
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  1998-12

4.  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

5.  Dentinogenesis imperfecta: genetic variations in a six-generation family.

Authors:  D Bixler; P M Conneally; A G Christen
Journal:  J Dent Res       Date:  1969 Nov-Dec       Impact factor: 6.116

Review 6.  Hereditary dentin defects.

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

7.  Dentinogenesis imperfecta: the importance of early treatment.

Authors:  Antonio Carlos Delgado; Matilde Ruiz; Jose Antonio Alarcón; Encarnación González
Journal:  Quintessence Int       Date:  2008-03       Impact factor: 1.677

8.  Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta.

Authors:  D A McKnight; J P Simmer; P S Hart; T C Hart; L W Fisher
Journal:  J Dent Res       Date:  2008-12       Impact factor: 6.116

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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  4 in total

1.  Dentinogenesis imperfecta type II: A case report with 17 years of follow-up.

Authors:  Francisco José Reis Gama; Isabella Sousa Corrêa; Claudia Scigliano Valerio; Emanuelle de Fátima Ferreira; Flávio Ricardo Manzi
Journal:  Imaging Sci Dent       Date:  2017-06-22

2.  Osteogenesis imperfecta: potential therapeutic approaches.

Authors:  Maxime Rousseau; Jean-Marc Retrouvey
Journal:  PeerJ       Date:  2018-08-17       Impact factor: 2.984

3.  Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.

Authors:  Kawther Taleb; Eva Lauridsen; Jette Daugaard-Jensen; Pekka Nieminen; Sven Kreiborg
Journal:  Mol Genet Genomic Med       Date:  2018-03-06       Impact factor: 2.183

4.  X-ray microanalysis of dentine in primary teeth diagnosed Dentinogenesis Imperfecta type II.

Authors:  N Sabel; J G Norén; A Robertson; D H Cornell
Journal:  Eur Arch Paediatr Dent       Date:  2019-12-10
  4 in total

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