"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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1996 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2006 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2011 | 1 | 1 | 2 |
2013 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Micrognathism" by people in Profiles.
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Phenotype of two Polish patients with Schaaf-Yang syndrome confirmed by identifying mutation in MAGEL2 gene. Clin Dysmorphol. 2018 Apr; 27(2):49-52.
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The Pierre Robin Mandible is Hypoplastic and Morphologically Abnormal. J Craniofac Surg. 2017 Nov; 28(8):1946-1949.
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Does Mandibular Distraction Vector Influence Airway Volumes and Outcome? J Oral Maxillofac Surg. 2017 Jan; 75(1):167-177.
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PDCD10 (CCM3) regulates brain endothelial barrier integrity in cerebral cavernous malformation type 3: role of CCM3-ERK1/2-cortactin cross-talk. Acta Neuropathol. 2015 Nov; 130(5):731-50.
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Molecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally. Prenat Diagn. 2014 Feb; 34(2):163-7.
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Finding disease variants in Mendelian disorders by using sequence data: methods and applications. Am J Hum Genet. 2011 Dec 09; 89(6):701-12.
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Temporomandibular joint replacement for ankylosis correction in Nager syndrome: case report and review of the literature. J Oral Maxillofac Surg. 2012 Mar; 70(3):616-25.
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Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female. Cytogenet Genome Res. 2009; 126(3):305-12.
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Severe proliferative congenital temporomandibular joint ankylosis: a proposed treatment protocol utilizing distraction osteogenesis. J Craniofac Surg. 2006 May; 17(3):605-10.
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Distraction osteogenesis of the mandible with an internal bioresorbable device. J Craniofac Surg. 2003 Sep; 14(5):791-6.