Dentinogenesis Imperfecta : A Family which was Affected for Over Three Generations
Dentinogenesis Imperfecta (DI) or hereditary opalescent dentin is inherited in a simple autosomal dominant mode with high penetrance and low mutation rates. It generally affects both the deciduous and the permanent dentitions. DI corresponds to a localized form of mesodermal dysplasia which is obs...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
JCDR Research and Publications Private Limited
2013-08-01
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| Series: | Journal of Clinical and Diagnostic Research |
| Subjects: | |
| Online Access: | https://jcdr.net/articles/PDF/3286/91-%205723_PF1(M)_E(C)_F(T)_F1(V)_F1(T)_PF1(VRP)_PFA(PR)_PF3_(PUH)_B.pdf |