"Anodontia" 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 the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed)
| Descriptor ID |
D000848
|
| MeSH Number(s) |
C07.650.800.100 C07.793.700.100 C16.131.850.800.100
|
| Concept/Terms |
Tooth Agenesis, Familial- Tooth Agenesis, Familial
- Ageneses, Familial Tooth
- Agenesis, Familial Tooth
- Familial Tooth Ageneses
- Familial Tooth Agenesis
- Tooth Ageneses, Familial
- Tooth Agenesis, Selective, 1
- Hypodontia Oligodontia 1
- Hypodontia Oligodontia 1s
- Oligodontia 1, Hypodontia
- Oligodontia 1s, Hypodontia
|
Below are MeSH descriptors whose meaning is more general than "Anodontia".
Below are MeSH descriptors whose meaning is more specific than "Anodontia".
This graph shows the total number of publications written about "Anodontia" by people in this website by year, and whether "Anodontia" 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 |
|---|
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Anodontia" by people in Profiles.
-
Doolan BJ, Onoufriadis A, Kantaputra P, McGrath JA. WNT10A, dermatology and dentistry. Br J Dermatol. 2021 12; 185(6):1105-1111.
-
Stone Hirsh L, Greco PM, Laudenbach JB, Atlas AM. Fusion of a Maxillary Central and Lateral Incisor With a Congenitally Missing Lateral: A 10-Year Conservative, Esthetic Approach. Compend Contin Educ Dent. 2017 Jan; 38(1):29-35; quiz 36.
-
Tziotzios C, Petrof G, Liu L, Verma A, Wedgeworth EK, Mellerio JE, McGrath JA. Clinical features and WNT10A mutations in seven unrelated cases of Sch?pf-Schulz-Passarge syndrome. Br J Dermatol. 2014 Nov; 171(5):1211-4.
-
Khurana VK, Gupta RK, Kumar LP. Witkop syndrome: A case report of an affected family. Dermatol Online J. 2012 Jun 15; 18(6):2.
-
Granger RH, Marshman G, Liu L, McGrath JA. Late diagnosis of ectodermal dysplasia syndrome. Australas J Dermatol. 2013 Feb; 54(1):46-8.
-
Gass JK, Wilson NJ, Smith FJ, Lane EB, McLean WH, Rytina E, Salvary I, Burrows NP. Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation. Br J Dermatol. 2009 Dec; 161(6):1396-8.
-
Winkler S, Boberick KG, Braid S, Wood R, Cari MJ. Implant replacement of congenitally missing lateral incisors: a case report. J Oral Implantol. 2008; 34(2):115-8.