Literature DB >> 10368575

[Dentinogenesis imperfecta. Scanning electron microscopic study and microanalysis].

E Salvolini1, R Di Giorgio, E Caselli, L De Florio.   

Abstract

BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects both the primary and secondary dentitions. Shields et al. in 1973 suggested a classification of DI within three types: type I, associated with osteogenesis imperfecta (OI), type II and type III. Although the varying clinical, radiographic and histological findings in DI have been described in detail, an available method for closer examination of the abnormal dentine matrix, electron microscopy, has seldom been used. Scanning and transmission electron microscopy studies can help to understand the pathogenesis of the different types of heritable dentine defects and the diagnosis and classification of these diseases. The aim of the present study was to evaluate a case of DI using scanning electron microscopy and microanalysis.
METHODS: Dentine was obtained from tooth samples from a fourteen-year-old boy affected by DI and from third molars extracted for therapeutic reasons used as controls. Samples were observed with a scanning electron microscope, scanning electron micrographs were evaluated with an image analysis program and specimens were finally observed with a scanning electron microscope equipped for micro-analysis. RESULTS AND
CONCLUSIONS: The results obtained showed that the total number of dentinal tubules was significantly reduced and the presence of a dentine mineralization defect in the patient affected by DI, in comparison to the controls.

Entities:  

Mesh:

Year:  1999        PMID: 10368575

Source DB:  PubMed          Journal:  Minerva Stomatol        ISSN: 0026-4970


  3 in total

1.  Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21.

Authors:  M L Beattie; J-W Kim; S-G Gong; C A Murdoch-Kinch; J P Simmer; J C-C Hu
Journal:  J Dent Res       Date:  2006-04       Impact factor: 6.116

2.  Immunocytochemical detection of dentin matrix proteins in primary teeth from patients with dentinogenesis imperfecta associated with osteogenesis imperfecta.

Authors:  G Orsini; A Majorana; A Mazzoni; A Putignano; M Falconi; A Polimeni; L Breschi
Journal:  Eur J Histochem       Date:  2014-12-01       Impact factor: 3.188

3.  Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype-phenotype correlation.

Authors:  M Chetty; T Roberts; S Shaik; P Beighton
Journal:  BDJ Open       Date:  2019-04-11
  3 in total

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