Results 11 to 20 of about 2,550 (192)
Esthetic-based Dental Management of Dentinogenesis Imperfecta in a 2.5-year-old Child [PDF]
Journal of Kerman University of Medical Sciences, 2021 Background: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, which occurs in the absence of any systemic disorder. The patients with DI presented rapid and severe attrition in primary teeth, which causes functional
Leyli Sadri +3 more
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Dentinogenesis imperfecta [PDF]
Medizinische Genetik, 2007 Zusammenfassung Unter Dentinogenesis imperfecta versteht man eine kongenitale Dysplasie des Dentins, die isoliert oder im Zusammenhang mit einer hereditären Allgemeinerkrankung wie der Osteogenesis imperfecta auftreten kann. Sie wird meist autosomal dominant vererbt und manifestiert sich klinisch in einer opaleszierenden Goldbraun- oder ...
Schulte, J M, Van Waes, H
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Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report [PDF]
Frontiers in Dentistry, 2016 Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi +2 more
doaj +2 more sources
Genetic Aspects of Dentinogenesis Imperfecta
Journal of Dentistry Indonesia, 2015 Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormalities in the dentin of the developing teeth and occurring at a rate of about 1 in 8000 births.
Elza Ibrahim Auerkari, Hedijanti Joenoes
doaj +3 more sources
Unravelling the Genetic Basis of Dentinogenesis Imperfecta
International Dental Journal, 2023 Aim or Purpose: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disorder affecting dentine formation. This study aimed to perform mutational analysis in individuals with DI to unravel its molecular mechanisms.
Dr Maleeha Gilani +1 more
doaj +2 more sources
Restorative Management of Dentinogenesis Imperfecta in an adult - A case report
Nigerian Dental Journal, 2020 Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permanent dentition. First described in the late 19th century, it is characterized by discolored and translucent teeth ranging from grey to brownish-blue or ...
A.O. Awotile, L.L. Enone, A. Oyapero
doaj +3 more sources
Prevalence of Dentinogenesis Imperfecta in a French Population. [PDF]
J Int Soc Prev Community Dent, 2017 Dentinogenesis imperfecta is a genetic disorder of the dentin occurring during the tooth development. It leads to many structural changes that can be identified clinically (brownish colored teeth, cracked enamel) and radiologically (globular crown, cervical constriction, short roots, and obliterated pulp chamber and/or root canals).
Cassia A +4 more
europepmc +4 more sources
European Journal of Histochemistry, 2014 Dentinogenesis imperfecta determines structural alterations of the collagen structure still not completely elucidated. Immunohistochemical analysis was used to assay Type I and VI collagen, various non-collagenous proteins distribution in human primary ...
G. Orsini +6 more
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Phenotypic Properties of Collagen in Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta [PDF]
International Journal of Nanomedicine, 2019 Salwa Ibrahim,1,* Adam P Strange,2,* Sebastian Aguayo,2,3 Albatool Shinawi,1 Nabilah Harith,1 Nurjehan Mohamed-Ibrahim,1 Samera Siddiqui,2 Susan Parekh,1 Laurent Bozec4 1Department of Paediatric Dentistry, UCL Eastman Dental Institute, University College
Ibrahim S +8 more
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Journal of Indian Academy of Oral Medicine and Radiology, 2003 Osteogenesis Imperfecta is a genetic disorder affecting approximately 20,000 U.S. population with multiple fracture of the bone. The, actual literature of the number of patients suffering from Osteogenesis Impcrfecta in Indian Population is still nor ...
Prabal Pal
doaj +1 more source