Name | Dentinogenesis Imperfecta |
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Synonyms | Capdepont Teeth | Dentinogenesis Imperfecta 1 | Dentinogenesis Imperfecta, Shields Type 2 | Dentinogenesis Imperfecta, Shields Type II | Dentinogenesis Imperfecta without Osteogenesis Imperfecta | Dentin, Opalescent | DGI1 | DGI-II | Hereditary Opalescent Dentin | Imperfecta 1, Dentinogenesis | Imperfecta, Dentinogenesis | Opalescent Dentin | Opalescent Dentin, Hereditary | Opalescent Teeth without Osteogenesis Imperfecta | Teeth, Capdepont |
Definition | An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated. |
Categories | Congenital abnormality | Mouth disease |
MeSH® ID | D003811 |
OMIM® ID | 125490 |
External Links |
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Diseases
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Stomatognathic Diseases
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Diseases
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Stomatognathic Diseases
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3. |
Diseases
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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