 Arthrogryposis
"Arthrogryposis" 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.
Persistent flexure or contracture of a joint. (Dorland, 27th ed)
| Descriptor ID |
D001176
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| MeSH Number(s) |
C05.550.150 C05.651.102 C05.660.077 C16.131.621.077
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| Concept/Terms |
Arthrogryposis- Arthrogryposis
- Arthrogryposes
- Myodystrophia Fetalis Deformans
- Arthromyodysplasia, Congenital
- Guerin-Stern Syndrome
- Guerin Stern Syndrome
- Syndrome, Guerin-Stern
- Amyoplasia Congenita
- Congenital Arthromyodysplasia
- Arthromyodysplasias, Congenital
- Congenital Arthromyodysplasias
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Below are MeSH descriptors whose meaning is more general than "Arthrogryposis".
Below are MeSH descriptors whose meaning is more specific than "Arthrogryposis".
This graph shows the total number of publications written about "Arthrogryposis" by people in this website by year, and whether "Arthrogryposis" 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 |
|---|
| 1990 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2009 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2019 | 2 | 0 | 2 |
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Below are the most recent publications written about "Arthrogryposis" by people in Profiles.
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Magini P, Smits DJ, Vandervore L, Schot R, Columbaro M, Kasteleijn E, van der Ent M, Palombo F, Lequin MH, Dremmen M, de Wit MCY, Severino M, Divizia MT, Striano P, Ordonez-Herrera N, Alhashem A, Al Fares A, Al Ghamdi M, Rolfs A, Bauer P, Demmers J, Verheijen FW, Wilke M, van Slegtenhorst M, van der Spek PJ, Seri M, Jansen AC, Stottmann RW, Hufnagel RB, Hopkin RJ, Aljeaid D, Wiszniewski W, Gawlinski P, Laure-Kamionowska M, Alkuraya FS, Akleh H, Stanley V, Musaev D, Gleeson JG, Zaki MS, Brunetti-Pierri N, Cappuccio G, Davidov B, Basel-Salmon L, Bazak L, Shahar NR, Bertoli-Avella A, Mirzaa GM, Dobyns WB, Pippucci T, Fornerod M, Mancini GMS. Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis. Am J Hum Genet. 2019 10 03; 105(4):689-705.
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Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. Eur J Med Genet. 2020 Jan; 63(1):103624.
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Ravenscroft G, Di Donato N, Hahn G, Davis MR, Craven PD, Poke G, Neas KR, Neuhann TM, Dobyns WB, Laing NG. Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria. Neuromuscul Disord. 2016 11; 26(11):744-748.
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Attali R, Warwar N, Israel A, Gurt I, McNally E, Puckelwartz M, Glick B, Nevo Y, Ben-Neriah Z, Melki J. Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis. Hum Mol Genet. 2009 Sep 15; 18(18):3462-9.
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Veugelers M, Bressan M, McDermott DA, Weremowicz S, Morton CC, Mabry CC, Lefaivre JF, Zunamon A, Destree A, Chaudron JM, Basson CT. Mutation of perinatal myosin heavy chain associated with a Carney complex variant. N Engl J Med. 2004 Jul 29; 351(5):460-9.
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Alward WL, Krachmer JH, Macsai MS. Arthrogryposis multiplex congenita with Peter's anomaly. J Pediatr Ophthalmol Strabismus. 1990 Nov-Dec; 27(6):329.
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