Diversity of clinical, radiographic and genealogical findings in 41 families with amelogenesis imperfecta
Author:
Affiliation:
1. Universidad de Chile, Chile; U-Odontología: Red de Investigación en Enfermedades Orales Complejas, Chile
2. Universidad de Chile, Chile
Publisher
FapUNIFESP (SciELO)
Subject
General Dentistry
Link
http://www.scielo.br/pdf/jaos/v27/1678-7765-jaos-27-e20180359.pdf
Reference30 articles.
1. Amelogensis imperfecta: a classification and catalogue for the 21st century;Aldred MJ;Oral Dis,2003
2. Amelogenesis imperfecta;Crawford PJ;Orphanet J Rare Dis,2007
3. Novel missense mutation of the FAM83H gene causes retention of amelogenin and a mild clinical phenotype of hypocalcified enamel;Urzúa B;Arch Oral Biol,2015
4. Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports;Toupenay S;BMC Oral Health,2018
5. A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement;Prasad MK;J Med Genet,2016
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3. Hereditary Tooth Anomalies: Amelogenesis Imperfecta, Dentinogenesis Imperfecta, Dentine Dysplasia;Dentistry;2024-07-17
4. Interdisciplinary full mouth rehabilitation of a patient with amelogenesis imperfecta from childhood to young adult‐hood: A 12‐year case report;Clinical Case Reports;2024-03
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