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Amelogenesis imperfecta (AI) is a diverse collection of inherited diseases that exhibit tooth enamel defects in the absence of systemic manifestations. Also known by various names such as Hereditary enamel dysplasia, Hereditary brown enamel, Hereditary brown opalescent teeth. It is an entirely ectodermal disturbance as mesenchymal components of teeth are basically normal.
The AI 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.
"AMELOGENESIS IMPERFECTA", International Journal for Research Trends and Innovation (www.ijrti.org), ISSN:2455-2631, Vol.7, Issue 6, page no.1304 - 1306, June-2022, Available :http://www.ijrti.org/papers/IJRTI2206197.pdf
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2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator