Amelogenesis imperfecta (AI) is a genetic disorder affecting enamel development affecting its structure and clinical appearance. It can affect both primary and/or permanent teeth and may be linked with nephrocalcinosis. Autosomal dominant inheritance is the main transmission mode of AI, but autosomal recessive, X-linked can also occur in some cases. AI is a serious condition that can result in reduced oral health-related quality of life and causes some psychological disturbance This article presents a case report of a partially edentulous patient with amelogenesis imperfecta along with its features.
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Aguir et al. (2024) studied this question.
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