Amelogenesis Imperfecta– 3 Cases
M. Anitha, Br. Sathvikalakshmi, A. Feroz Khan, R. Sudharshan
Journal of Advances in Medical and Pharmaceutical Sciences · pp. 1–8 · Published 22 Sep 2018
10.9734/JAMPS/2018/39759Abstract
Amelogenesis imperfecta (AI) - a hereditary heterogenous disorder causing developmental alterations in the structure of enamel. The Al trait can be transmitted by either autosomal dominant, autosomal recessive, or X-linked modes of inheritance. Genes implicated in autosomal forms are genes encoding enamel matrix proteins, namely: Enamelin and Ameloblastin, Tuftelin, MMP-20 and Kallikrein – 4 [1]. It is necessary to diagnose the case and provide durable functional and esthetic management of these patients, where the unaesthetic appearance has a definite negative psychological impact. We present here three case reports of AI that we diagnosed on the basis of clinical and radiographic features along with the complete review.
Cited by 2
Adeline Le Cabec, Thomas Colard, Damien Charabidze · Scientific Reports · 2021
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