Abstract
Amelogenesis imperfecta (AI) is related to a group of developmental tooth abnormalities (also referred as hereditary dysplasia), which affect the genome of the individual and retard at least one of the stages of enamel formation. AI is, in general, a hereditary disorder with clinical impact on both deciduous and permanent teeth. Patients with AI often complain of tooth sensitivity, difficulty in chewing, self-consciousness about the appearance of their teeth, and an anterior open bite. We present a case report of AI (hypocalcified), which was diagnosed based on classical clinical and radiographic features.