Amelogenesis Imperfecta - A Case Report with Genetic Transmission
نویسندگان
چکیده
Amelogenesis imperfecta (AI) is a hereditary disorder expressing a group of conditions that cause developmental alterations in the structure of enamel. AI is a serious problem that reduces oral health-related quality of life and causes some physiological problems. The treatment of patients with AI may upgrade the quality of life and reinforce their self-esteem. The Al trait can be transmitted by either autosomal dominant, autosomal recessive, or X-linked modes of inheritance. It is necessary to diagnose the case and provide durable functional and esthetic management of these patients in order to improve the quality of their lives. We present a case of amelogenesis imperfecta affecting the dentition of a 36 year old male which was inherited by his 3 year old daughter.
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Amelogenesis Imperfecta with Taurodontism, Microdontia, and Minor Thalassemia: A Case Report
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