Results 81 to 90 of about 2,550 (192)

Dentinogenesis imperfecta type II: case report.

, 1996
A case of dentinogenesis imperfecta type II is described. The authors also present a brief literature review and focus on the difficulty in treating such cases.\ud ...
Modesto, A, Portella, W, Alves, A C, Vieira, A R   +3 more
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TYPE II DENTINOGENESIS IMPERFECTA : CASE REPORT

, 2001
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the histodifferentiation stage of tooth development, with involvement of the primary and permanent teeth.
이제호, 최병재
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Early Rehabilitation of Incisors with Dentinogenesis Imperfecta Type II – Case Report

, 2017
Dentinogenesis imperfecta is an phenotypic alteration in the formation of the organic matrix. It causes the rapid and progressive wear of tooth structure, which may compromise tooth function and aesthetics.
Maíra Mery Rosa, Ana Paula CA Beltrame, Ricardo AT Noschang, Izabel CS Almeida   +3 more
core   +1 more source

A Novel Mutation in the DSPP Gene Associated with Dentinogenesis Imperfecta Type II

, 2009
Hereditary dentin defects are divided into dentinogenesis imperfecta and dentin dysplasia. We identified a family segregating severe dentinogenesis imperfecta.
Jeon, D., Lee, H., Lee, S.-H., Lee, G., Jung, Y.-J., Lee, K.-E., Kim, J.-W., Shin, C.-U., Hahn, S.-H., Lee, S.-K.   +9 more
core   +1 more source

THE CONTRIBUTION OF KINETIC THERAPY IN LOBSTEIN’S DISEASE [PDF]

Annals of the “Ştefan cel Mare” University: Physical Education and Sport Section - The Science and Art of Movement, 2018
Osteogenesis imperfecta is a genetic disease of the connective tissue whose main clinical sign is increased bone fragility, manifested especially through fractures of the long limbs. OI presents major clinical signs and minor clinical signs.
Sergiu Danail, Danelciuc Francisc Tadeus
doaj  

Dentinogenesis imperfecta Type II. Case report

, 2014
La Dentinogénesis Imperfecta (DI) es una alteración hereditaria originada en la etapa de histodiferenciación de la odontogénesis. Existen dos tipos de Dentinogénesis Imperfecta, la tipo I, asociada a osteogénesis imperfecta, y la tipo II en la cual los ...
Guevara, Carlos, Álvarez, Giancarlos, Jerez, Elsy, Omaña Cepeda, Carlos Javier   +3 more
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Alternative treatment for dentinogenesis imperfecta

Revista Cubana de Estomatología, 2015
Introduction: Dentinogenesis imperfecta is an autosomal dominant hereditary disease originated in the stage of histodiferenciation during the odontogenesis, it´s a form of a localized mesodermic dysplasia, characterized by alteration of dentinal proteins.
Mirta Elena Montero del Castillo, Yanet Casals González, Lourdes Valdés Barroso   +2 more
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FAMILY SURVEILLANCE OF OSTEOGENESIS IMPERFECTA: PREGNANCY OUTCOMES, TACTICAL APPROACHES, AND PROSPECTS FOR SOLVING THE PROBLEM

Мать и дитя в Кузбассе, 2023
Osteogenesis imperfecta is a rare, hereditary, genetically heterogeneous disease of connective tissue and skeleton caused by mutation of genes encoding collagen, osteoblast differentiation, bone tissue remodulator proteins and many other genes.
Сергей Васильевич Матошин, Светлана Владимировна Шрамко   +1 more
doaj  

Dentinogenesis Imperfecta: Relationship of Genotype with Clinical and Radiographic Features

, 2010
Dentinogenesis Imperfecta (DGI) is the most common hereditary anomaly of human dentin. It is typically diagnosed by clinical and radiographic features. It occurs in isolation or in conjunction with the syndrome osteogenesis imperfecta.
Shahangian, Seyed Jossein
core   +1 more source

Dentinogenesis Imperfecta Type I and II: A Case Series Highlighting Clinical and Radiographic Insights

Indian Journal of Dental Sciences
Dentinogenesis imperfecta (DI) is a rare hereditary disorder affecting the dentin structure of both primary and permanent teeth, characterized by discoloration, structural fragility, and distinctive radiographic features.
K. Kavitha, Parikh J. Shilpa, Shah S. Jigna   +2 more
doaj   +1 more source