Results 91 to 100 of about 14,453 (188)
Alternative treatment for dentinogenesis imperfecta
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 +2 more
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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 +1 more
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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 +2 more
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Dental Findings and Treatment in Osteogenesis Imperfecta: A Case Report
Osteogenesis imperfecta (OI) is a genetically inherited disease in which increased bone fragility, low bone mass, and connective tissue disorders are seen. In other words, 'glass bone disease'; has been associated with blue sclera, hearing problems, hand-
Yasemin İspir, Özge Anıl
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Rehabilitation of an attrited dentition is one of the most challenging task faced by a prosthodontist which requires a systematic, phase wise approach. Hobo’s techniques and Pankey Mann Schuyler’s philosophy are widely used and documented for full mouth ...
Amina +4 more
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Compromised alveolar bone cells in a patient with dentinogenesis imperfecta caused by DSPP mutation
International audienceDentin sialophosphoprotein (DSPP) plays an important role in the mineralization of both dentin and bones. The Dspp null mice developed periodontal diseases. Patients with DSPP mutations have dentinogenesis imperfecta (DGI), but very
Thantrira Porntaveetus +19 more
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Osteogenesis imperfecta associated with dentinogenesis imperfecta
Objetivo: O presente trabalho tem como objetivo fazer uma revisão da literatura sobre as manifestações orais da Osteogênese Imperfeita. Metodologia: Revisão integrativa da literatura, qualitativa de cunho descritiva e foram utilizadas as bases de dados SciELO - Scientific Eletronic Library Online, a PubMed- National Library of Medicine e a Plataforma ...
Azevedo, Marcelle Jayne Santos +3 more
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Students with Osteogenesis Imperfecta: A Comparative Intergenerational Study of Inclusive Participation in New Zealand schools. [PDF]
Osteogenesis imperfecta (OI) is a genetic condition commonly known as Brittle Bones. The purpose of this study was to listen to and document the experiences of those with OI to investigate if there were barriers to inclusive education for students with ...
Holmes, Heather Jeanette
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Osteogenesis imperfecta, a case report
Introduction: osteogenesis imperfecta or crystal bones constitute the hereditary osteoporotic syndrome with the highest incidence in childhood. Case report: a 6-year and three-month-old school student admitted to the pediatric intensive care unit with a
Lázaro Raidel Moreira-Díaz +2 more
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