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Print ISSN:-2395-4914

Online ISSN:-2395-499X

CODEN : IJOHC8

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Year 2020

Volume: 6 , Issue: 1

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International Journal of Oral Health Dentistry


Amelogenesis Imperfecta: A case report


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Author Details : Sandeep Kaur, Kirandeep Kaur, Neha Mahajan, Abhiroop Singh, Romesh Singh

Volume : 3, Issue : 1, Year : 2017

Article Page : 70-73


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Abstract

Amelogenesis Imperfecta(AI) represents structural developmental defect of tooth enamel having complex inheritance pattern. 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. Here, we report three cases among six children of the same family with Amologenesis imperfecta, analyse the clinical presentation, diagnostic features and clinical complications of Amelogenesis imperfecta.

Keywords:
Amelogenesis imperfecta, Discoloration, Hypoplastic, Hypomaturative

How to cite : Kaur S, Kaur K, Mahajan N, Singh A, Singh R, Amelogenesis Imperfecta: A case report. Int J Oral Health Dent 2017;3(1):70-73

Copyright © 2017 by author(s) and Int J Oral Health Dent. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC-BY-NC 4.0) (creativecommons.org)