"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 |
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2001 | 0 | 1 | 1 |
2002 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2013 | 1 | 0 | 1 |
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 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Micrognathism" by people in Profiles.
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Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish. Dis Model Mech. 2023 06 01; 16(6).
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Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia. Am J Med Genet A. 2022 09; 188(9):2718-2723.
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Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathies. Genet Med. 2022 02; 24(2):364-373.
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Two-Stage Treatment of a Large Premaxillary Defect. J Craniofac Surg. 2021 Nov-Dec 01; 32(8):2827-2829.
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Mandibular Distraction in Robin Sequence With Multi-Level Airway Disease: Always Contraindicated? J Craniofac Surg. 2020 Oct; 31(7):1883-1887.
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Predictive Factors for Perinatal Outcomes of Infants Diagnosed With Micrognathia Antenatally. Ear Nose Throat J. 2021 Jan; 100(1):NP16-NP20.
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Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4. Mol Genet Genomic Med. 2019 06; 7(6):e682.
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Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. Am J Hum Genet. 2019 01 03; 104(1):164-178.
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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.