ArticleCureus2024
Partial Amelogenesis Imperfecta: A Report of a Rare Case.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Amelogenesis imperfecta is a collection of genetic disorders that impair the structure of dental enamel. The condition presents in a variety of ways, affecting enamel development, mineralization, and maturation. Amelogenesis imperfecta can follow various inheritance patterns, including autosomal dominant, autosomal recessive, sex-linked, and sporadic. This case report describes a 22-year-old female diagnosed with amelogenesis imperfecta. The patient's clinical presentation, diagnostic process, and comprehensive treatment approaches are discussed, emphasizing the importance of multidisciplinary care in improving functional and esthetic outcomes. Treatment is ongoing and aims to improve both functional and esthetic outcomes. This case report details the presentation, characteristic radiographic findings, and management discussion of a patient presented with a rare condition that is termed "partial amelogenesis imperfecta."
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