 Tooth Abnormalities
"Tooth Abnormalities" 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.
Congenital absence of or defects in structures of the teeth.
| Descriptor ID |
D014071
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| MeSH Number(s) |
C07.650.800 C07.793.700 C16.131.850.800
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| Concept/Terms |
Tooth Abnormalities- Tooth Abnormalities
- Abnormalities, Tooth
- Abnormality, Tooth
- Tooth Abnormality
- Teeth Abnormalities
- Abnormalities, Teeth
- Abnormality, Teeth
- Teeth Abnormality
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Below are MeSH descriptors whose meaning is more general than "Tooth Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Tooth Abnormalities".
This graph shows the total number of publications written about "Tooth Abnormalities" by people in this website by year, and whether "Tooth Abnormalities" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 | | 2011 | 2 | 1 | 3 | | 2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Tooth Abnormalities" by people in Profiles.
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Daoud H, Tétreault M, Gibson W, Guerrero K, Cohen A, Gburek-Augustat J, Synofzik M, Brais B, Stevens CA, Sanchez-Carpintero R, Goizet C, Naidu S, Vanderver A, Bernard G. Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism. J Med Genet. 2013 Mar; 50(3):194-7.
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Hsieh DT, Chang T. Incontinentia pigmenti: skin and magnetic resonance imaging findings. Arch Neurol. 2011 Aug; 68(8):1080.
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Kantaputra P, Tanpaiboon P, Porntaveetus T, Ohazama A, Sharpe P, Rauch A, Hussadaloy A, Thiel CT. The smallest teeth in the world are caused by mutations in the PCNT gene. Am J Med Genet A. 2011 Jun; 155A(6):1398-403.
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Sripathomsawat W, Tanpaiboon P, Heering J, Dötsch V, Hennekam RC, Kantaputra P. Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome. Am J Med Genet A. 2011 Jan; 155A(1):228-32.
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Kantaputra PN, Tanpaiboon P, Unachak K, Praphanphoj V. Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome. Am J Med Genet A. 2004 Oct 01; 130A(2):181-90.
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