"Dental Enamel Hypoplasia" 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 acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
| Descriptor ID |
D003744
|
| MeSH Number(s) |
C07.650.800.255 C07.793.700.255 C16.131.850.800.255
|
| Concept/Terms |
Dental Enamel Hypoplasia- Dental Enamel Hypoplasia
- Hypoplastic Enamel
- Enamel, Hypoplastic
- Enamel Hypoplasia, Dental
- Hypoplasia, Dental Enamel
- Enamel Agenesis
- Ageneses, Enamel
- Agenesis, Enamel
- Enamel Ageneses
- Enamel Hypoplasia
- Enamel Hypoplasias
- Hypoplasia, Enamel
- Hypoplasias, Enamel
|
Below are MeSH descriptors whose meaning is more general than "Dental Enamel Hypoplasia".
Below are MeSH descriptors whose meaning is more specific than "Dental Enamel Hypoplasia".
This graph shows the total number of publications written about "Dental Enamel Hypoplasia" by people in this website by year, and whether "Dental Enamel Hypoplasia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
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Below are the most recent publications written about "Dental Enamel Hypoplasia" by people in Profiles.
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P?rez A, Almaani N, Stefanato CM, BhogaL B, Groves RW, Mellerio JE, McGrath JA. Bullous pemphigoid in a patient with suspected non-Herlitz junctional epidermolysis bullosa. Clin Exp Dermatol. 2010 Dec; 35(8):881-4.
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Musa FU, Ratajczak P, Sahu J, Pentlicky S, Fryer A, Richard G, Willoughby CE. Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43). Eye (Lond). 2009 Mar; 23(3):549-55.
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Murrell DF, Pasmooij AM, Pas HH, Marr P, Klingberg S, Pfendner E, Uitto J, Sadowski S, Collins F, Widmer R, Jonkman MF. Retrospective diagnosis of fatal BP180-deficient non-Herlitz junctional epidermolysis bullosa suggested by immunofluorescence (IF) antigen-mapping of parental carriers bearing enamel defects. J Invest Dermatol. 2007 Jul; 127(7):1772-5.
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McGrath JA, Gatalica B, Li K, Dunnill MG, McMillan JR, Christiano AM, Eady RA, Uitto J. Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition. Am J Pathol. 1996 Jun; 148(6):1787-96.