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- W2894269843 abstract "Amelogenesis imperfecta is an ectodermal alteration with a hereditary character that manifests as an alteration in the tooth enamel in both the dental arcades, with no occurrences of systemic disorders, where genes that code the enamel proteins are mutated. They are characterized by extensive loss of tooth enamel tissue, without alterations in the dental pulp, which can cause tooth sensitivity, the loss of vertical dimension and aesthetic compromise, with psychological and social sequelae. The teeth look rougher, with a higher tendency of plaque accumulation and occurrence of gingivitis. This study aimed to report the case of a 12-year-old boy, feoderm, who after the anamnesis, clinical examination, and imaging tests was found to have amelogenesis imperfecta, hypoplastic type. The planning and proposed multidisciplinary treatment aim to achieve the aesthetic, functional, psychological, and social rehabilitation for this patient." @default.
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- W2894269843 date "2018-09-01" @default.
- W2894269843 modified "2023-09-27" @default.
- W2894269843 title "Amelogenesis Imperfecta: a Case Report" @default.
- W2894269843 doi "https://doi.org/10.1016/j.oooo.2018.02.476" @default.
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