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Review Article 1 2 3 4 Peeyush Shivhare , Lata Shankarnarayan , Ashish Gupta , Pulivarthi Sushma 1 2 Department of Oral Medicine and Radiology, Narsinhbhai Patel Dental College and Hospital, Visnagar, Gujarat, India, Department of Oral Medicine and Radiology, Rungta College of Dental Sciences and Research, Bhilai, Chhattisgarh, India, Department of Oral Medicine and Radiology, Department of Department of Oral Medicine and Radiology, Rajarajeswri Dental College and Hospital, Bengaluru, Karnataka, India ABSTRA CT Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit quantitative or qualitative tooth enamel defects in the absence of systemic manifestations. This entity can present a variety of clinical presentation varies from hypoplastic, hypomaturative to hypocalcified which are the result of various genetic mutations. AI can present with a vast variety of features in single entity, so detailed knowledge of genetic mutations regarding AI, diagnostic, radiographic features, and different treatment modalities are mandatory while dealing these cases. We are presenting a review article on AI, mainly focused on its clinical presentation, genetic background, and its treatment modalities. Keywords: Amelogenesis imperfecta, dominant, enamel, recessive of enamel and hypoplastic-hypomaturation with INTRODUCTION [1] taurodontism [Table 1]. Amelogenesis imperfecta (AI) is an inherited disorder Hypoplastic AI
Journal of Advanced Oral Research – SAGE
Published: Jan 1, 2016
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