Literature review of amelogenesis imperfecta with case report

Amelogenesis impertecta (Al) is a diverse collection of inherited diseases that exhibit qualitative or quantitative tooth enamel defects in the absence of systemic manifestations. Also known by varied names, such as hereditary enamel dysplasia, hereditary brown opalescent teeth, this defect is entir...

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Main Authors: Sumathy C Chanmougananda, Kannan A Ashokan, Seethalakshmi C Ashokan, Anitha B Bojan, Ragu M Ganesh
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Journal of Indian Academy of Oral Medicine and Radiology
Subjects:
Online Access:http://www.jiaomr.in/article.asp?issn=0972-1363;year=2012;volume=24;issue=1;spage=83;epage=87;aulast=Chanmougananda
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author Sumathy C Chanmougananda
Kannan A Ashokan
Seethalakshmi C Ashokan
Anitha B Bojan
Ragu M Ganesh
author_facet Sumathy C Chanmougananda
Kannan A Ashokan
Seethalakshmi C Ashokan
Anitha B Bojan
Ragu M Ganesh
author_sort Sumathy C Chanmougananda
collection DOAJ
description Amelogenesis impertecta (Al) is a diverse collection of inherited diseases that exhibit qualitative or quantitative tooth enamel defects in the absence of systemic manifestations. Also known by varied names, such as hereditary enamel dysplasia, hereditary brown opalescent teeth, this defect is entirely ectodermal, since mesodermal components of the teeth are basically normal. This article details a case of Al along with complete review which presents in his twin siblings with clinical, radiological and histopathological report.
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spelling doaj.art-65421d639034477b9b2867bc4bb443762022-12-21T23:31:08ZengWolters Kluwer Medknow PublicationsJournal of Indian Academy of Oral Medicine and Radiology0972-13630975-15722012-01-01241838710.5005/jp-journals-10011-1266Literature review of amelogenesis imperfecta with case reportSumathy C ChanmouganandaKannan A AshokanSeethalakshmi C AshokanAnitha B BojanRagu M GaneshAmelogenesis impertecta (Al) is a diverse collection of inherited diseases that exhibit qualitative or quantitative tooth enamel defects in the absence of systemic manifestations. Also known by varied names, such as hereditary enamel dysplasia, hereditary brown opalescent teeth, this defect is entirely ectodermal, since mesodermal components of the teeth are basically normal. This article details a case of Al along with complete review which presents in his twin siblings with clinical, radiological and histopathological report.http://www.jiaomr.in/article.asp?issn=0972-1363;year=2012;volume=24;issue=1;spage=83;epage=87;aulast=ChanmouganandaAmelogenesis imperfectaMutationEnamel proteaseInherited disease
spellingShingle Sumathy C Chanmougananda
Kannan A Ashokan
Seethalakshmi C Ashokan
Anitha B Bojan
Ragu M Ganesh
Literature review of amelogenesis imperfecta with case report
Journal of Indian Academy of Oral Medicine and Radiology
Amelogenesis imperfecta
Mutation
Enamel protease
Inherited disease
title Literature review of amelogenesis imperfecta with case report
title_full Literature review of amelogenesis imperfecta with case report
title_fullStr Literature review of amelogenesis imperfecta with case report
title_full_unstemmed Literature review of amelogenesis imperfecta with case report
title_short Literature review of amelogenesis imperfecta with case report
title_sort literature review of amelogenesis imperfecta with case report
topic Amelogenesis imperfecta
Mutation
Enamel protease
Inherited disease
url http://www.jiaomr.in/article.asp?issn=0972-1363;year=2012;volume=24;issue=1;spage=83;epage=87;aulast=Chanmougananda
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