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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Dentinogenesis imperfecta type III with dentinogenesi and cementum defects. Dentinogenesis Imperfecta DI represents one of those abnormalities inherited in a dominant autosomic pattern.

Scopus See more Follow us: A review and case report of a family over four generations. Sequence determination of an extremely acidic rat dentin phosphoprotein.

CiteScore measures average citations received per document published. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisted: Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfect. Dentinogenesis imperfecta in the Brandywine isolate: Dentinogenis Imperfecta Type II: Under a Creative Commons license.

J Am Dent Assoc,pp. Unusual dentinal changes in dentinogenesis imperfecta associated with osteogenesis imperfecta. J Dent Child, 48pp. Hereditary opalescent dentine Dentinogenesis Imperfecta.

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

SJR uses a similar algorithm as the Dehtinogenesis page rank; it provides a quantitative and qualitative measure of the journal’s impact. Oral rehabilitation in dentinogenesis imperfecta with overdentures.


Discrimination of morphological findings in osteogenesis imperfecta patients using combination of polarized light microscopy, microradiography and scanning electron microscopy. Denitnogenesis imperfecta DGI is one of the most common hereditary disorders of dentin formation. Genetic linkage of dentinogenesis imperfecta Type III locus to chromosome 4q. Dentin phosphoprotein DNA sequence determination. A proposed classification for heritable human dentine defect with a description of a new entity.

Professor Auxiliar na Universidade Fernando Pessoa. Am J Orthod Oral Surg, 25pp. J Dent Res, 86pp. J Dent Res ; Si continua navegando, consideramos que acepta su uso.

Either or both primary and permanent dentition is affected by it.

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

J Oral Pathol Med, 34pp. Cells Tissues Organs,pp. SRJ is a prestige metric based on the idea that not all citations are the same. You can change the settings or obtain more information by clicking here. Shafer’s textbook of oral pathology. Further studies, for certain, are extremely required to finally elucidate the outlines of imperfectta dramatic dental condition. Malmgren B, Lindskog S. Int J Pediatr Dent ;9: This article has been cited by.

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

This item has received. Inorganic phase in dentinogenesis imperfecta. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin. J Dent Res, 88pp. Indian J Dent Res ; The Iowa Fluoride Study X.

Dentin phosphoprotein DNA sequence determination. Discontinued publication For more information click here. Clinical radiologic and scanning electron microscopic studies of the dentition.

Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4: Dentinogenesis is a highly controlled process that results in the encompassed mineralization of the predentin into a mineralized matrix. Arch Oral Biol ; Are you a health professional able to prescribe or dispense drugs?

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. Ultrastructure of dental tissues in dentinogenesis imperfecta in man.