Amelogenesis Imperfecta: A Case Report and Review of Literature

被引：1

作者：

Nigam, Pankhuri ^{[1
]}

Singh, Vijay Pal ^{[2
]}

Prasad, Krishna Deo ^{[1
]}

Tak, Jalaj ^{[1
]}

机构：

[1] Shree Bankey Bihari Dent Coll & Res Ctr, Dept Oral & Maxillofacial Pathol & Microbiol, Ghaziabad, Uttar Pradesh, India

[2] Shree Bankey Bihari Dent Coll & Res Ctr, Dept Orthodont & Dentofacial Orthopaed, Ghaziabad, Uttar Pradesh, India

来源：

INTERNATIONAL JOURNAL OF SCIENTIFIC STUDY | 2015年 / 2卷 / 10期

关键词：

Amelogenesis imperfecta; Enamel; Hereditary; Management; Treatment;

D O I：

10.17354/ijss/2015/36

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

Amelogenesis imperfecta (AI) is a hereditary disorder that causes developmental alterations in the structure of enamel. It represents a group of heterogenous conditions. AI has several names such as hereditary enamel dysplasia, hereditary brown enamel, hereditary brown opalescent teeth. In this disorder, the enamel is hypoplastic, hypomineralized or both. It may show autosomal dominant, autosomal recessive, sex-linked or sporadic pattern. It is necessary to diagnose this disorder and provide durable, functional and esthetic management of these patients to improve the quality of their lives. We present a case of AI affecting the dentition of an 18-year-old girl.

引用

页码：146 / 149

页数：4

共 12 条

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