 Micrognathism
"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.
Unusual or undue smallness of the jaws. (Dorland, 27th ed)
| Descriptor ID |
D008844
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| 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
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| Concept/Terms |
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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 |
|---|
| 1996 | 1 | 0 | 1 | | 2003 | 1 | 0 | 1 | | 2006 | 0 | 1 | 1 | | 2010 | 0 | 1 | 1 | | 2011 | 1 | 1 | 2 | | 2013 | 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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Matuszewska KE, Badura-Stronka M, Smigiel R, Cabala M, Biernacka A, Kosinska J, Rydzanicz M, Winczewska-Wiktor A, Sasiadek M, Latos-Bielenska A, Zemojtel T, Ploski R. 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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Zellner EG, Reid RR, Steinbacher DM. The Pierre Robin Mandible is Hypoplastic and Morphologically Abnormal. J Craniofac Surg. 2017 Nov; 28(8):1946-1949.
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Zellner EG, Mhlaba JM, Reid RR, Steinbacher DM. Does Mandibular Distraction Vector Influence Airway Volumes and Outcome? J Oral Maxillofac Surg. 2017 Jan; 75(1):167-177.
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Dempsey MA, Knight Johnson AE, Swope BS, Moldenhauer JS, Sroka H, Chong K, Chitayat D, Briere L, Lyon H, Palmer N, Gopalani S, Siebert JR, Lévesque S, Leblanc J, Menzies D, Haverfield E, Das S. Molecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally. Prenat Diagn. 2014 Feb; 34(2):163-7.
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Ionita-Laza I, Makarov V, Yoon S, Raby B, Buxbaum J, Nicolae DL, Lin X. 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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Schlieve T, Almusa M, Miloro M, Kolokythas A. 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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Hulick PJ, Noonan KM, Kulkarni S, Donovan DJ, Listewnik M, Ihm C, Stoler JM, Weremowicz S. 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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Bartlett SP, Reid RR, Losee JE, Quinn PD. 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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Margulis A, Patel PK, Daw JL, Bauer BS. Distraction osteogenesis of the mandible with an internal bioresorbable device. J Craniofac Surg. 2003 Sep; 14(5):791-6.
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Chin M, Toth BA. Distraction osteogenesis in maxillofacial surgery using internal devices: review of five cases. J Oral Maxillofac Surg. 1996 Jan; 54(1):45-53; discussion 54.
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