Rootless teeth: Dentin dysplasia type I
A rare case of hereditary disturbance of dentine, Dentin dysplasia type I is presented, which is characterized by short or total absence of roots, obliterated pulp chambers, and peri-apical radiolucencies. It affects both primary and secondary dentition. Management of patients with dentinal dysplasi...
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Main Authors: | , |
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Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2013-01-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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Summary: | A rare case of hereditary disturbance of dentine, Dentin dysplasia type I is presented, which is characterized by short or total absence of roots, obliterated pulp chambers, and peri-apical radiolucencies. It affects both primary and secondary dentition. Management of patients with dentinal dysplasia is difficult and requires a multidisciplinary approach. An overview of dentin dysplasia and its management along with a case report is discussed. |
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Item Description: | 0976-237X 0976-2361 10.4103/0976-237X.123063 |