Literature DB >> 11447953

Dentinogenesis imperfecta: an early treatment strategy.

S Sapir1, J Shapira.   

Abstract

Dentinogenesis imperfecta (DI) type 2 is a disease inherited in a simple autosomal dominant mode. As soon as the teeth erupt the parents may notice the problem and look for a pediatric dentist's advice and treatment. Early diagnosis and treatment of DI is recommended, as it may prevent or intercept deterioration of the teeth and occlusion and improve esthetics. The purpose of this article is to present the objectives, treatment options, and problems encountered in the treatment of DI in the early primary dentition. A two-stage treatment of a toddler under general anesthesia is described and discussed. This paper recommends for severe cases of DI two treatment stages performed under general anesthesia. Stage 1 is early (around age 18-20 months) and is directed to covering the incisors with composite restorations and the first primary molars with preformed crowns. Stage 2 (around age 28-30 months) seeks to protect the second primary molars with preformed crowns and cover the canines with composite restorations.

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Year:  2001        PMID: 11447953

Source DB:  PubMed          Journal:  Pediatr Dent        ISSN: 0164-1263            Impact factor:   1.874


  13 in total

1.  Dentinogenesis Imperfecta : A Family which was Affected for Over Three Generations.

Authors:  Poornima Surendra; Rohan Shah; Roshan N M; V V Subba Reddy
Journal:  J Clin Diagn Res       Date:  2013-08-01

Review 2.  Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.

Authors:  Muriel de La Dure-Molla; Benjamin Philippe Fournier; Ariane Berdal
Journal:  Eur J Hum Genet       Date:  2014-08-13       Impact factor: 4.246

Review 3.  Tooth dentin defects reflect genetic disorders affecting bone mineralization.

Authors:  S Opsahl Vital; C Gaucher; C Bardet; P S Rowe; A George; A Linglart; C Chaussain
Journal:  Bone       Date:  2012-01-26       Impact factor: 4.398

4.  Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.

Authors:  Jung-Wook Kim; Jan C-C Hu; Jae-Il Lee; Sung-Kwon Moon; Young-Jae Kim; Ki-Taeg Jang; Sang-Hoon Lee; Chong-Chul Kim; Se-Hyun Hahn; James P Simmer
Journal:  Hum Genet       Date:  2004-12-08       Impact factor: 4.132

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

Authors:  C Millet; S Viennot; J P Duprez
Journal:  Eur Arch Paediatr Dent       Date:  2010-10

6.  Clinical manifestations and dental management of dentinogenesis imperfecta associated with osteogenesis imperfecta: Case report.

Authors:  Halima Abukabbos; Faisal Al-Sineedi
Journal:  Saudi Dent J       Date:  2013-11-07

7.  Dentinogenesis imperfecta type II: Diagnosis, functional and esthetic rehabilitation in mixed dentition.

Authors:  Ramneet Kaur; Asha Karadwal; Deepak Sharma; Manpreet Kaur Sandhu
Journal:  J Oral Maxillofac Pathol       Date:  2021-03-19

Review 8.  Amelogenesis imperfecta.

Authors:  Peter J M Crawford; Michael Aldred; Agnes Bloch-Zupan
Journal:  Orphanet J Rare Dis       Date:  2007-04-04       Impact factor: 4.123

9.  Dentinogenesis imperfecta type I: A case report with literature review on nomenclature system.

Authors:  D Devaraju; Bk Yashoda Devi; Vijeev Vasudevan; V Manjunath
Journal:  J Oral Maxillofac Pathol       Date:  2014-09

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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