Dentinogenesis Imperfecta
"Dentinogenesis Imperfecta" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D003811
|
| MeSH Number(s) |
C07.650.800.270 C07.793.700.270 C16.131.850.800.270
|
| Concept/Terms |
Opalescent Dentin- Opalescent Dentin
- Dentin, Opalescent
- Dentinogenesis Imperfecta 1
- Imperfecta 1, Dentinogenesis
- Capdepont Teeth
- Teeth, Capdepont
- Dentinogenesis Imperfecta, Shields Type II
|
Below are MeSH descriptors whose meaning is more general than "Dentinogenesis Imperfecta".
Below are MeSH descriptors whose meaning is more specific than "Dentinogenesis Imperfecta".
This graph shows the total number of publications written about "Dentinogenesis Imperfecta" by people in this website by year, and whether "Dentinogenesis Imperfecta" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Dentinogenesis Imperfecta" by people in Profiles.
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Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice. Stem Cells Dev. 2019 05 15; 28(10):683-694.
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[Osteogenesis imperfecta associated with dentinogenesis imperfecta]. Stomatologia (Athenai). 1979 Mar-Apr; 36(2):90-4.