"Micrognathism" 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.
Abnormally small jaw.
| Descriptor ID |
D008844
|
| MeSH Number(s) |
C05.500.460.457 C05.660.207.540.460.457 C07.320.440.457 C07.650.500.460.457 C16.131.621.207.540.460.457 C16.131.850.500.460.457
|
| Concept/Terms |
Micrognathism- Micrognathism
- Micrognathisms
- Mandibular Micrognathism
- Mandibular Micrognathisms
- Micrognathism, Mandibular
- Micrognathisms, Mandibular
- Micrognathia
- Micrognathias
- Congenital Micrognathism
- Congenital Micrognathisms
- Micrognathism, Congenital
- Micrognathisms, Congenital
- Congenital Micrognathia
- Congenital Micrognathias
- Micrognathia, Congenital
- Micrognathias, Congenital
- Mandibular Micrognathia
- Mandibular Micrognathias
- Micrognathia, Mandibular
- Micrognathias, Mandibular
|
Below are MeSH descriptors whose meaning is more general than "Micrognathism".
Below are MeSH descriptors whose meaning is more specific than "Micrognathism".
This graph shows the total number of publications written about "Micrognathism" by people in this website by year, and whether "Micrognathism" 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 |
|---|
| 2001 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2013 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 1 | 2 |
| 2016 | 1 | 2 | 3 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 2 | 2 |
| 2019 | 2 | 0 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 2 | 0 | 2 |
| 2022 | 3 | 0 | 3 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
| 2025 | 1 | 0 | 1 |
| 2026 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Micrognathism" by people in Profiles.
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BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes. Nat Commun. 2018 11 20; 9(1):4885.
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Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability. Hum Mutat. 2017 10; 38(10):1365-1371.
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De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms. Am J Hum Genet. 2016 Oct 06; 99(4):934-941.
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A probabilistic disease-gene finder for personal genomes. Genome Res. 2011 Sep; 21(9):1529-42.
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Clinical outcome of fetuses with sonographic diagnosis of isolated micrognathia. Obstet Gynecol. 2003 Oct; 102(4):801-5.
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Three-dimensional ultrasonographic presentation of micrognathia. J Ultrasound Med. 2002 Jul; 21(7):775-81.