Amelogenesis Imperfecta – Case Series and Management

Q2 Dentistry
Rishi Tyagi Prof, Namita Kalra Prof Hod, Amit Khatri Asso Prof, Harsh Singh Pg, Mayank Sharma Pg, Puja Sabherwal Pg
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引用次数: 0

Abstract

Amelogenesis imperfecta (AI) incorporates an assemblage of hereditary diseases that involve the defective formation or calcification of enamel. Also known by varied names such as Hereditary enamel dysplasia, Hereditary brown enamel, Hereditary brown opalescent teeth, this defect is entirely ectodermal, since mesodermal components are unaffected. AI is typically characterized by generalized enamel defects in both primary and permanent dentition. The AI trait can be transmitted by either autosomal dominant, autosomal recessive, or X-linked modes of inheritance.AI has a marked impact on aesthetics, function and psychology of the patient. Early intervention and dental rehabilitation should be carried out with strong emphasis on the preventive care and strict follow up schedule. Key words: Amelogenesis imperfecta, developmental anomaly, Dental Rehabilitation
无胚性发育不全:病例系列和处理
无釉质发育不全症(AI)包括一系列涉及釉质形成缺陷或钙化的遗传性疾病。也被称为不同的名称,如遗传性牙釉质发育不良,遗传性棕色牙釉质,遗传性棕色乳白色牙齿,这种缺陷完全是外胚层的,因为中胚层成分不受影响。AI的典型特征是在初级和永久牙列中出现全身性牙釉质缺损。人工智能性状可以通过常染色体显性、常染色体隐性或x连锁遗传模式传播。人工智能对患者的审美、功能和心理都有显著的影响。应进行早期干预和牙齿康复,重点是预防保健和严格的随访计划。关键词:无胚性发育不全;发育异常;口腔康复
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来源期刊
Journal of Clinical Dentistry
Journal of Clinical Dentistry Dentistry-Dentistry (all)
CiteScore
3.40
自引率
0.00%
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0
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