Enamel hypoplasia or amelogenesis imperfecta - a restorative approach
نویسندگان
چکیده
Rodrigo Borges Fonseca1 Lourenço Correr Sobrinho2 Alfredo Júlio Fernandes Neto3 Adérito Soares da Mota3 Carlos José Soares4 1DDS, MS, Graduate student at Piracicaba Dental School, State University of Campinas – São Paulo, Brazil. 2DDS, MS, PhD, Professor at Piracicaba Dental School, State University of Campinas – São Paulo, Brazil. 3DDS, MS, PhD, Professor at Dental School, Federal University of Uberlândia – Minas Gerais, Brazil. 4DDS, MS, PhD, Professor at Dental School, Federal University of Uberlândia – Minas Gerais, Brazil.
منابع مشابه
Multidisciplinary Approach for Restoring Function and Esthetics in a Patient with Amelogenesis Imperfecta: A Clinical Report
Amelogenesis imperfecta has been defined as a group of hereditary enamel defects which may or may not be associated with some other dental and skeletal developmental defects. It can be characterized by enamel hypoplasia, hypomaturation, or hypo-calcification of the teeth. This clinical report describes the oral rehabilitation of a twenty two year old female patient with amelogenesis imperfecta ...
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Amelogenesis imperfecta is an inherited disease that disturbs the formation of the enamel. It occurs as two main categories, hypomineralized and hypoplastic. Both deciduous and permanent teeth are affected, and the disorder may create unaesthetic appearance, dental sensitivity, and severe attrition. In this article through performing a structured literature review, numerous treatment modalities...
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Amelogenesis imperfecta (AI) has been defined as a group of hereditary enamel defects. It can be characterized by enamel hypoplasia, hypomaturation, or hypocalcification of the teeth. AI may be associated with some other dental and skeletal developmental defects. Restoration for patients with this condition should be oriented toward the functional and esthetic rehabilitation. This clinical repo...
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Tricho-dento-osseous (TDO) syndrome is a rare, autosomal dominant disorder principally characterised by curly hair at infancy, severe enamel hypomineralization and hypoplasia and taurodontism of teeth, sclerotic bone, and other defects. Diagnostic criteria are based on the generalized enamel defects, severe taurodontism especially of the mandibular first permanent molars, an autosomal dominant ...
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Amelogenesis imperfecta is a group of inherited diseases affecting the quality and quantity of dental enamel. To date, mutations in more than ten genes have been associated with non-syndromic amelogenesis imperfecta (AI). Among these, ENAM and LAMB3 mutations are known to be parts of the etiology of hypoplastic AI in human cases. When both alleles of LAMB3 are defective, it could cause junction...
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