A rare condition affecting the primary and permanent dentition: Dentin dysplasia type I
Dentin dysplasia type I is a genetic defect of dentin formation, which is inherited as an autosomal dominant trait. In this anomaly, the teeth generally appear unremarkable with normal crowns; and it is characterized by normal appearing crowns, absence or severe restriction of root formation, oblite...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2013-01-01
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| Series: | Journal of Oral and Maxillofacial Radiology |
| Subjects: | |
| Online Access: | http://www.joomr.org/article.asp?issn=2321-3841;year=2013;volume=1;issue=1;spage=13;epage=16;aulast=Sekerci |