"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 |
|---|
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 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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Nephrocalcinosis in Amelogenesis Imperfecta Caused by the FAM20A Mutation. Nephron. 2018; 139(2):189-196.
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Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene. Eur J Med Genet. 2018 Jul; 61(7):384-387.
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A novel AMELX mutation causes hypoplastic amelogenesis imperfecta. Arch Oral Biol. 2017 Apr; 76:61-65.
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Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes. Oral Surg Oral Med Oral Pathol Oral Radiol. 2017 Feb; 123(2):229-234.e2.