The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of Review; Open Access. clinical section. Dentinogenesis imperfecta: an early treatment strategy Dentinogenesis imperfecta (DI) type 2 is a disease inherited in .. prehensive review. PDF | Dentinogenesis imperfecta (DI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal dominant.

Author: Faule Tushakar
Country: Philippines
Language: English (Spanish)
Genre: Personal Growth
Published (Last): 5 November 2008
Pages: 438
PDF File Size: 9.40 Mb
ePub File Size: 13.82 Mb
ISBN: 841-8-79710-937-5
Downloads: 6143
Price: Free* [*Free Regsitration Required]
Uploader: Goltidal

Management of dentinogenesis imperfecta: a review of two case reports.

Either or both primary and permanent dentition is affected by it. Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4. Orban’s Oral histology and embryology, 11th ed.

It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin. Revew improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.


A review and case report of a family over four generations.

Professor Associado na Universidade Fernando Pessoa. Sequence determination of an extremely acidic rat dentin phosphoprotein. RGO, 48pp.

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

Continuing navigation will be considered as acceptance of this use. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Further studies, for certain, are extremely required to finally elucidate the outlines of this dramatic dental condition.

Discrimination of morphological findings in osteogenesis imperfecta patients using combination of polarized light microscopy, microradiography and scanning electron microscopy. Malmgren B, Lindskog S.

To understand the molecular basis of this disorder, as well as, its clinical and radiographic evidences, it is essential to make an appropriate diagnosis and ulterior treatment. Are you a health professional able to prescribe or dispense drugs?

How to cite this article: Management of opalescent dentin: Scanning electron microscopy of teeth in osteogenesis imperfecta type I. This article has been cited by. Subscribe to our Newsletter. J Am Dent Assoc,pp. Previous article Next article. SRJ is a prestige metric based on the idea that not all citations are the same.


Imperfectz imperfecta associated with short stature, hearing loss and mental retardation: Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed dentinoogenesis a single transcript coded by a gene on human chromosome 4: Dentinogenesis imperfecta in the Brandywine isolate: You can change the settings or obtain more information by clicking here. J Dent Res, 86pp. Scopus See more Follow us: Arch Oral Biol ; Dentinogenesis imperfecta type III with enamel and cementum defects.

Management of dentinogenesis imperfecta: a review of two case reports.

Unusual dentinal changes in dentinogenesis imperfecta associated with osteogenesis imperfecta. None, Conflict of Interest: Prakash H, Joshi N. SJR uses a similar algorithm as the Google page rank; it provides dentinoyenesis quantitative and qualitative measure of the journal’s impact. Autosomal dominant, dentinogenesis imperfecta, dystrophic dentin, mesodermal defect, pulpal space obliteration.

Professor Auxiliar na Universidade Fernando Pessoa. Indian J Dent Res ; Tatiana Cardoso a ,??