Results 231 to 240 of about 6,417 (245)
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Oral Surgery, Oral Medicine, Oral Pathology, 1963
Abstract 1. 1. The dental symptoms presented by the two cases reported here are compatible with the classic descriptions of enamel hypoplasia, enamel hypocalcification, and associated osteogenesis imperfecta. 2. 2. Because of the hereditary nature of the condition, the clinical and roentgenographic signs may serve as a guide in treatment ...
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Abstract 1. 1. The dental symptoms presented by the two cases reported here are compatible with the classic descriptions of enamel hypoplasia, enamel hypocalcification, and associated osteogenesis imperfecta. 2. 2. Because of the hereditary nature of the condition, the clinical and roentgenographic signs may serve as a guide in treatment ...
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Amelogenesis imperfecta: the orthodontic perspective
British Dental Journal, 2012Orthodontics in patients with amelogenesis imperfecta can be complicated by commonly occurring dental features in this group as well as patient factors. In this article we examine ways to avoid the common pitfalls of orthodontic management and the importance of adequate and timely liaison between the general dental practitioner and the ...
L. Currie +4 more
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Oral Surgery, Oral Medicine, Oral Pathology, 1975
Amelogenesis imperfecta demonstrating the classic mendelian heredity factor is reported in two members of the same family.
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Amelogenesis imperfecta demonstrating the classic mendelian heredity factor is reported in two members of the same family.
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Therapy for amelogenesis imperfecta
The Journal of Prosthetic Dentistry, 1959S TUDIES OF AMELqGENESIS IMPERFECTA~-~ have revealed two types of enamel dysplasias : hereditary enamel hypoplasia and hereditary enamel hypocalcification. In hereditary enamel hypoplasia there is a thin layer of mature enamel with a hard, smooth, glossy surface. The yellow color of the dentine is visible through the thin enamel and the crowns are cone
Peter Simon, John F. Prichard
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A noninvasive treatment of amelogenesis imperfecta.
Quintessence international (Berlin, Germany : 1985), 2013Amelogenesis imperfecta is a hereditary disease affecting the quality and quantity of enamel with a prevalence of 1:700 to 1:14,000. Patients suffer from dental sensitivity and compromised esthetics. The conservative treatment of choice is based on ceramic crowns, but preparation design is unnecessarily destructive to tooth tissue.
Uwe Blunck +2 more
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Analysis of a kindred with amelogenesis imperfecta
Journal of Oral Pathology & Medicine, 1985Amelugenesis imperfecta (A1) is a group of hereditary disorders whose manifestations are generally considered as being confined to the teeth. Pedigree analysis of a kindred revealed 2 siblings affected with AI which was consistent with an autosomal recessive mode of inheritance.
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Oral Surgery, Oral Medicine, Oral Pathology, 1968
Jack Prince, Gilbert E. Lilly
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Jack Prince, Gilbert E. Lilly
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Amelogenesis imperfecta: The genetics, classification, and treatment
The Journal of Prosthetic Dentistry, 1983Abstract A short review of genetics pertinent to amelogenesis imperfecta was presented along with a review of its various means of classification. A multidisciplinary treatment involving orthodontics, periodontics, and prosthodontics was presented.
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The human genetics of amelogenesis imperfecta
2010Amelogenesis imperfecta (AI) results from the mutation of gene(s) that affect enamel development. The resulting enamel may have alterations of enamel quantity, composition, and/or structure and typically appears abnormally thin, soft, rough, and/or stained.
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Sex Ratio in Amelogenesis Imperfecta
Journal of Dental Research, 1976Wendy Simm, Denys H. Goose
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