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: Shakakora Mazushicage
Country: Gambia
Language: English (Spanish)
Genre: Video
Published (Last): 4 September 2006
Pages: 241
PDF File Size: 10.43 Mb
ePub File Size: 10.58 Mb
ISBN: 180-5-37214-807-2
Downloads: 55324
Price: Free* [*Free Regsitration Required]
Uploader: Fesar

Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisted: J Dent Res ; Professor Auxiliar na Universidade Fernando Pessoa.

Intrafibrillar mineral may be absent in dentinogenesis imperfecta type II. Are you a health professional able to prescribe or dispense drugs? Si continua navegando, consideramos que acepta su uso.

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

Further studies, for certain, are extremely required to finally elucidate the outlines of this dramatic dental condition. Dentin phosphoprotein DNA sequence determination.

Rajendran R, Sivapathasundram B, editors. Shafer’s textbook of oral pathology. Acta Odontol Scand ; J Dent Res, 88pp.


J Clin Pediatr Dent ; Subscribe to our Newsletter. Bhandari S, Pannu K.

How to cite this URL: You can change the settings or obtain more information by clicking here. J Oral Pathol ; None, Conflict of Interest: Dentinogenesis imperfecta in the Brandywine isolate: Discrimination of morphological findings in osteogenesis imperfecta patients using combination of polarized light microscopy, microradiography and scanning electron microscopy.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. This article has been cited by. J Dent Res, 85pp. A proposed classification for heritable human dentine defects with a description of a new entity.

Full text is only aviable in PDF. Birth defects, 7pp. Imperfefta navigation will be considered as acceptance of this use. Prakash H, Joshi N. Print Send to a friend Export reference Mendeley Statistics. J Am Dent Assoc ; Orban’s Oral histology and embryology, 11th ed. Dentinogenesis imperfecta associated with short stature, hearing loss and mental retardation: Professor Associado na Universidade Fernando Pessoa.

Autosomal dominant, dentinogenesis imperfecta, dystrophic dentin, mesodermal defect, pulpal space obliteration. J Biol Chem ; Dentin phosphoprotein DNA sequence determination. J Dent Child, 48pp. How to cite this article: Dentinogenesis Imperfecta DI dentinogwnesis one of those abnormalities inherited in a dominant autosomic pattern. J Biol Chem,pp.


J Dentinotenesis Pathol Dentinogeenesis, 34pp.

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

Dentinogenis Imperfecta Type II: Indian J Dent Res ; Oral rehabilitation in dentinogenesis imperfecta with overdentures. Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfect. The Iowa Fluoride Study. Previous article Next article. Treatment of Dentinogenesis Imperfecta in a child. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin.

A text book of oral pathology, WB Saunders Co, 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. Developmental disturbances of oral and paraoral structures. Arch Oral Biol, 18pp.