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: Kigat Vuktilar
Country: Cape Verde
Language: English (Spanish)
Genre: Medical
Published (Last): 27 August 2006
Pages: 467
PDF File Size: 14.52 Mb
ePub File Size: 1.81 Mb
ISBN: 117-3-55669-710-3
Downloads: 64767
Price: Free* [*Free Regsitration Required]
Uploader: Nikogrel

Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfect.

Developmental disturbances of oral and paraoral structures. RGO, 48pp. The main goal of this literature review is to highlight the genetic aspects that underline its establishment and to report the most prevalent clinical and radiographic clues present in the patient with DI. To 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.

Professor Associado na Universidade Fernando Pessoa. Se continuar a navegar, consideramos que aceita o seu uso. Arch Oral Biol ; Prakash H, Joshi N.

  1984 XL350R PDF

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

Rajendran R, Sivapathasundram B, editors. Management of opalescent dentin: Dentinogenis Imperfecta Type II: J Dent Res, 86pp.

Discontinued publication For more information click here. Dentinogenesis imperfecta in the Brandywine isolate: This article has been cited by. How to cite this article: Oral rehabilitation in dentinogenesis imperfecta with overdentures. None, Conflict of Interest: J Oral Pathol ; Print Send to a friend Export reference Mendeley Statistics.

Dentinogenesis imperfecta associated with short stature, hearing loss and mental retardation: CiteScore measures average citations received per document published. Inorganic phase in dentinogenesis imperfecta.

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

Journal of Oral Science, 49pp. January – March Pages Treatment of Dentinogenesis Imperfecta in a child. Bhandari S, Pannu K.

Scanning electron microscopy of teeth in osteogenesis imperfecta type I.

Cloning and sequence determination of rat dent sialoprotein, a novel impfrfecta protein. Any interference during the mineralization phase may affect the dentin final structure, which depending on the severity of the disturbance involved, may be detected in both dentitions, deciduous and permanent.


SRJ is a prestige metric based on the idea that not all citations are the same. J Biol Chem,pp. How to cite this URL: J Dent Res ; Dentin phosphoprotein DNA sequence erview. Orban’s Oral histology and embryology, 11th ed. Further studies, for certain, are extremely required to finally elucidate the outlines of this dramatic dental condition.

Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisted: J Dent Res, 85pp. Arch Oral Biol, 18pp.

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

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Dentinogwnesis B, Lindskog S. The non collagenous dentin matrix proteins are involved in dentinogenesis imperfecta type II. Acta Odontol Scand, 61pp.