Results 181 to 190 of about 4,054 (202)
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Pediatric dental management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta
Special Care in Dentistry, 2007ABSTRACTOsteogenesis imperfecta (OI) is a genetic disorder that affects all connective tissue. Clinical manifestations of OI include bone fragility, hyperlaxity of joints, hearing loss, abnormalities of stature and facial structure, blue scleras, and dentinogenesis imperfecta (DI).
Kelly A. Muhney, Patricia R. Campbell
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The ultrastructure of the dental tissues in dentinogenesis imperfecta in man
Archives of Oral Biology, 1985Eight primary incisors obtained from a child with dentinogenesis imperfecta (DI) type II were examined histologically using light microscopy and scanning electron microscopy. In both the DI and control teeth, large dentinal canals were observed along the midline of the crown distributed mesial-distally and coursing towards the pulp. Variably-structured
D.G. Gantt, John Tim Wright
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Multidisciplinary management of a case of dentinogenesis imperfecta
Indian Journal of Multidisciplinary Dentistry, 2015Preventive and restorative care are of utmost importance in the management of cases of dentinogenesis imperfecta in order to restore function, esthetics and also prevent further damage of the remaining dental tissues. The multidisciplinary approach would help to provide the optimal treatment outcome.
Sibu Sajjan Simon, Sajani Ramachandran
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Hereditary opalescent dentine (Dentinogenesis imperfecta)
American Journal of Orthodontics and Oral Surgery, 1939Abstract Several cases of hereditary opalescent dentine are described and analyzed histologically and genetically. The similarity in the dental changes in hereditary opalescent dentine and osteogenesis imperfecta is pointed out, and the characteristic effects are grouped under the general term “dentinogenesis imperfecta.”
Isaac Schour, E Roberts
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Linkage between dentinogenesis imperfecta and Gc
Annals of Human Genetics, 1982SUMMARYA large family with dentinogenesis imperfecta shows that this locus is linked to the Gc locus on chromosome 4q. The maximum lod score is + 7.9 at a male recombination fraction of 0.05 and female recombination fraction of 0.24.
K. E. Buckton +3 more
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Hereditary dentinogenesis imperfecta
The Journal of Pediatrics, 1959Orlen N. Johnson +9 more
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Dentinogenesis imperfecta: severe expression in a probable homozygote
Clinical Genetics, 1972A family wherein 25 individuals, of whom 23 are affected and 2 are reputed to be affected with dentinogenesis imperfecta, is presented. The distribution of the patients which spans 5 generations in this pedigree accords well with autosomal dominant transmission of the disorder. A consanguineous marriage of 2 second cousins both of whom are affected has
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The teeth in osteogenesis and dentinogenesis imperfecta
British Dental Journal, 1980E P Sunderland, C J Smith
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Osteogenesis imperfecta and dentinogenesis imperfecta
Australian Dental Journal, 1963B. Vern Barnett, A. Vern Barnett
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Dentinogenesis imperfecta: an interdisciplinary approach
British Dental Journal, 1988J M Battagel, M Levinkind
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