"Amelogenesis 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.
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
| Descriptor ID |
D000567
|
| MeSH Number(s) |
C07.650.800.255.500 C07.793.700.255.500 C16.131.850.800.255.500
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Amelogenesis Imperfecta".
Below are MeSH descriptors whose meaning is more specific than "Amelogenesis Imperfecta".
This graph shows the total number of publications written about "Amelogenesis Imperfecta" by people in this website by year, and whether "Amelogenesis Imperfecta" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Amelogenesis Imperfecta" by people in Profiles.
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The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):618-630.
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Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort. Am J Med Genet A. 2020 03; 182(3):493-497.