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.

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J Am Dent Assoc ; It follows an autosomal dentinotenesis pattern of transmission, affecting both the formation and mineralization of dentin. Am J Orthod Oral Surg, 25pp. Se continuar a navegar, consideramos que aceita o seu uso. Unusual dentinal changes in dentinogenesis imperfecta associated with osteogenesis imperfecta. Oral rehabilitation in dentinogenesis imperfecta with overdentures.

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

Malmgren B, Lindskog S. Discrimination of morphological findings in osteogenesis imperfecta patients using combination dentinovenesis polarized light microscopy, microradiography and scanning electron microscopy. Further studies, for certain, are extremely required to finally elucidate the outlines of this dramatic dental condition.


The Iowa Fluoride Study X.

Cells Tissues Organs,pp. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. This item has received. The non collagenous dentin matrix proteins are involved in dentinogenesis imperfecta type II. Arch Oral Biol ; J Am Dent Assoc,pp. Previous article Next article.

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

Full text is only aviable in PDF. 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. J Dent Res ; 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.

Under a Creative Commons license. Dentinogenesis imperfecta DGI is one of the most common hereditary disorders of dentin formation.

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

Genetic linkage of dentinogenesis imperfecta Type III locus to chromosome 4q. Si continua navegando, consideramos que acepta su uso. Dentin phosphoprotein DNA sequence determination. J Biol Chem,pp.


This article has been cited by. Either or both primary and permanent dentition is affected by it. Shafer’s textbook of oral pathology. Print Send to a friend Export reference Mendeley Statistics. The Iowa Fluoride Study. Indian J Dent Res ; Continuing navigation will be considered as acceptance of this use. Prakash H, Joshi N.

None, Conflict of Interest: Sequence determination of an extremely acidic rat dentin phosphoprotein. Acta Odontol Scand ; You can change the settings or obtain more information by clicking here. Bhandari S, Pannu K. Intrafibrillar mineral may be absent in dentinogenesis imperfecta type II. Dentinogenesis imperfecta type III with enamel and cementum defects.