ENAM Gene Mutation Factor in Amelogenesis Imperfecta

Anie Apriani, L. Sembiring, Ibnu Suryatmojo, F. Sandra
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Abstract

Amelogenesis Imperfecta (AI) is an abnormal disease that occurs in hard tissue of teeth. Clinical features of Amelogenesis Imperfecta look like immature enamel that looks like hypomaturation. The etiology of AI is influenced by the TGF-?1 factor which is disturbed during the formation and development of enamel, one of which is caused by the presence of ENAM gene mutations. Further research on genetic history in the family and biomineralization of the formation of  enamel important to be developed later.
无染色体发育不全的ENAM基因突变因子
无釉发育不全症是发生在牙齿硬组织中的一种异常疾病。无釉发育不全的临床特征为未成熟的牙釉质,看起来像低饱和度。AI的病因受TGF-?一种在牙釉质形成和发育过程中受到干扰的因子,其中之一是由ENAM基因突变引起的。对牙釉质形成的家族遗传史和生物矿化的进一步研究有待进一步开展。
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