Results 1 to 10 of about 4,054 (202)
Regenerative Endodontic Treatment in Dentinogenesis Imperfecta-Induced Apical Periodontitis. [PDF]
Case Rep DentPulp involvement of immature permanent teeth with dentinogenesis imperfecta is challenging and could lead to extraction. A case of dentinogenesis imperfecta-induced periapical periodontitis of an immature permanent tooth was treated with regenerative ...
Liao Y, Pan T, Xing X.
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Dentinogenesis imperfecta [PDF]
Medizinische Genetik, 2018 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.
Schulte, J.M., van Waes, H.
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Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia [PDF]
Orphanet Journal of Rare Diseases, 2008 The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and ...
Barron, Martin J +3 more
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Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children. [PDF]
Dent J (Basel), 2021 Osteogenesis imperfecta (OI) is a genetic disorder characterized by increased bone fragility and low bone mass, caused mainly by mutations in collagen type I encoding genes. The current study aimed to evaluate dentinogenesis imperfecta (DI), oral manifestations and caries status of OI children. Sixty-eight children (41 males, 27 females) aged from 3 to
Nguyen HTT +6 more
europepmc +6 more sources
Osteogenesis imperfecta and dentinogenesis imperfecta
Current Medicine Research and Practice, 2022 Osteogenesis imperfecta (OI) is a rare congenital condition, marked by fragile bones, skeletal deformities and additional extra-skeletal symptoms. Depending upon the degree of seriousness, affected people can either carry on with a mostly unrestricted, independent life, or their mobility is severely affected, making them ...
Chetna Grover +3 more
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Dentinogenesis imperfecta: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2008 Dentinogenesis imperfecta is an autosomal dominant disorder of tooth development characterized by the presence of opalescent dentin, resulting in a dusky blue to brownish discoloration of the teeth. This condition is genetically and clinically heterogeneous; it may affect only the teeth or it may be associated with the osteogenesis imperfecta ...
Sony Sugnani +2 more
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Prosthodontic rehabilitation of dentinogenesis imperfecta
Contemporary Clinical Dentistry, 2011 Dentinogenesis imperfecta and its prosthodontic management is a challenging task. Treatment protocol varies according to clinical case. Although various reports in the literature suggest general guidelines for treatment planning, the present case report describes a full mouth rehabilitation of a young patient with dentinogenesis imperfecta treated by ...
Anil Goud, Saee Deshpande
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Dentinogenesis imperfecta: The Genetic Causes and Outcomes [PDF]
The Cardinal Edge, 2021 Dentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth development irregularities, and decreased tooth strength. This autosomal dominant disorder is identified in individuals of all ages.
Johnson, Sydney P, Ms.
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Dentinogenesis imperfecta in a 6-year-old male neutered Labrador retriever: Case report with atypical clinical presentation and treatment review. [PDF]
Front Vet SciThis case report details the diagnosis and treatment of dentinogenesis imperfecta in a 6-year-old neutered male Labrador, presenting without concurrent osteogenesis imperfecta.
Piekos KM, Freeman A, Fleming K, Bell C.
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Clear Aligners in Patients with Amelogenesis and Dentinogenesis Imperfecta. [PDF]
Int J Dent, 2021 Dentinogenesis imperfecta (DI) and amelogenesis imperfecta (AI) are hereditary abnormalities of dental hard tissues. Dental abnormalities may also be accompanied by symptoms of disorders such as osteogenesis imperfecta. AI and DI have a significant burden on socializing, function, and comfort; therefore, frequent screening and accurate diagnosis is the
Sawan NM.
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