Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya

<p>Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalities in the dentin of developing teeth and occuring at a rate of about 1 in 8000 births affecting both primary and secondary dentitions. The expression of DI shows a high penetrance and a low...

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Main Authors: Elza Ibrahim Auerkari, A. Surjadi, S. Mangoendjaja
Format: Article
Language:English
Published: Faculty of Dentistry, Universitas Indonesia 2015-10-01
Series:Journal of Dentistry Indonesia
Online Access:http://jdentistry.ui.ac.id/index.php/JDI/article/view/814
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author Elza Ibrahim Auerkari
A. Surjadi
S. Mangoendjaja
author_facet Elza Ibrahim Auerkari
A. Surjadi
S. Mangoendjaja
author_sort Elza Ibrahim Auerkari
collection DOAJ
description <p>Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalities in the dentin of developing teeth and occuring at a rate of about 1 in 8000 births affecting both primary and secondary dentitions. The expression of DI shows a high penetrance and a low mutation rate. Two main types of DI appear to exist: type 1 which is the defect associate with osteogenesis imperfecta, and type II which is the classical hereditary opalescent dentin. The formerly proposed DI type III appears to be only a modified expression of the same gene as in the classical DI type II. This paper reviews molecular genetic aspects of DI.</p>
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spelling doaj.art-26e32c1971f144d7802aac8c294554ab2022-12-22T02:10:28ZengFaculty of Dentistry, Universitas IndonesiaJournal of Dentistry Indonesia1693-96972355-48002015-10-0162313610.14693/jdi.v6i2.814708Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya PenanggulangannyaElza Ibrahim Auerkari0A. Surjadi1S. Mangoendjaja2Department of Oral Biology, Faculty of Dentistry, Universitas Indonesia, Jakarta 10430Department of Oral Biology, Faculty of Dentistry, Universitas Indonesia, Jakarta 10430Department of Oral Biology, Faculty of Dentistry, Universitas Indonesia, Jakarta 10430<p>Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalities in the dentin of developing teeth and occuring at a rate of about 1 in 8000 births affecting both primary and secondary dentitions. The expression of DI shows a high penetrance and a low mutation rate. Two main types of DI appear to exist: type 1 which is the defect associate with osteogenesis imperfecta, and type II which is the classical hereditary opalescent dentin. The formerly proposed DI type III appears to be only a modified expression of the same gene as in the classical DI type II. This paper reviews molecular genetic aspects of DI.</p>http://jdentistry.ui.ac.id/index.php/JDI/article/view/814
spellingShingle Elza Ibrahim Auerkari
A. Surjadi
S. Mangoendjaja
Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
Journal of Dentistry Indonesia
title Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
title_full Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
title_fullStr Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
title_full_unstemmed Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
title_short Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
title_sort dentinogenesis imperfekta aspek genetika molekular klasifikasi dan upaya penanggulangannya
url http://jdentistry.ui.ac.id/index.php/JDI/article/view/814
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