 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.
| 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
- Arthromyodysplasia, Congenital
- Arthromyodysplasias, Congenital
- Congenital Arthromyodysplasias
- Congenital Arthromyodysplasia
- Guerin-Stern Syndrome
- Guerin Stern Syndrome
- Syndrome, Guerin-Stern
- Myodystrophia Fetalis Deformans
- Arthrogryposis Multiplex Congenita (AMC)
- Arthrogryposis Multiplex Congenitas (AMC)
- Congenita, Arthrogryposis Multiplex (AMC)
- Congenitas, Arthrogryposis Multiplex (AMC)
- Multiplex Congenita, Arthrogryposis (AMC)
- Multiplex Congenitas, Arthrogryposis (AMC)
- Fibrous Ankylosis of Multiple Joints
- Guérin-Stern Syndrome
- Guérin Stern Syndrome
- Syndrome, Guérin-Stern
- Otto Syndrome
- Syndrome, Otto
- Rocher-Sheldon Syndrome
- Rocher Sheldon Syndrome
- Syndrome, Rocher-Sheldon
- Rossi Syndrome
- Syndrome, Rossi
- Arthrogryposis Multiplex Congenita
- Arthrogryposis Multiplex Congenitas
- Congenita, Arthrogryposis Multiplex
- Congenitas, Arthrogryposis Multiplex
- Multiplex Congenita, Arthrogryposis
- Multiplex Congenitas, Arthrogryposis
- Amyoplasia Congenita
- Congenital Multiple Arthrogryposis
- Arthrogryposes, Congenital Multiple
- Arthrogryposis, Congenital Multiple
- Congenital Multiple Arthrogryposes
- Multiple Arthrogryposes, Congenital
- Multiple Arthrogryposis, Congenital
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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 |
|---|
| 2007 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2015 | 2 | 1 | 3 | | 2021 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Arthrogryposis" by people in Profiles.
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Giampietro PF, Hadley-Miller N, Raggio CL. Overview of Gene Special Issue "Genetic Conditions Affecting the Skeleton: Congenital, Idiopathic Scoliosis and Arthrogryposis". Genes (Basel). 2022 07 04; 13(7).
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Sions JM, Donohoe M, Beisheim-Ryan EH, Pohlig RT, Shank TM, Nichols LR. Characterizing Pain Among Adolescents and Young Adults With Arthrogryposis Multiplex Congenita. Pediatr Phys Ther. 2022 07 01; 34(3):288-295.
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Sions JM, Donohoe M, Beisheim-Ryan EH, Pohlig RT, Shank TM, Nichols LR. Test-retest reliability for performance-based outcome measures among individuals with arthrogryposis multiplex congenita. BMC Musculoskelet Disord. 2022 Feb 05; 23(1):121.
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Krack AT, Bernstein JA, Ruddy RM. Recognition, Evaluation, and Management of Pediatric Hereditary Angioedema. Pediatr Emerg Care. 2021 Apr 01; 37(4):218-223.
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Chong JX, Burrage LC, Beck AE, Marvin CT, McMillin MJ, Shively KM, Harrell TM, Buckingham KJ, Bacino CA, Jain M, Alanay Y, Berry SA, Carey JC, Gibbs RA, Lee BH, Krakow D, Shendure J, Nickerson DA, Bamshad MJ. Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3. Am J Hum Genet. 2015 May 07; 96(5):841-9.
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Chong JX, McMillin MJ, Shively KM, Beck AE, Marvin CT, Armenteros JR, Buckingham KJ, Nkinsi NT, Boyle EA, Berry MN, Bocian M, Foulds N, Uzielli ML, Haldeman-Englert C, Hennekam RC, Kaplan P, Kline AD, Mercer CL, Nowaczyk MJ, Klein Wassink-Ruiter JS, McPherson EW, Moreno RA, Scheuerle AE, Shashi V, Stevens CA, Carey JC, Monteil A, Lory P, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ. De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay. Am J Hum Genet. 2015 Mar 05; 96(3):462-73.
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Azbell K, Dannemiller L. A Case Report of an Infant With Arthrogryposis. Pediatr Phys Ther. 2015; 27(3):293-301.
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Jao LE, Appel B, Wente SR. A zebrafish model of lethal congenital contracture syndrome 1 reveals Gle1 function in spinal neural precursor survival and motor axon arborization. Development. 2012 Apr; 139(7):1316-26.
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Ho CA, Karol LA. The utility of knee releases in arthrogryposis. J Pediatr Orthop. 2008 Apr-May; 28(3):307-13.
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Murphy AM, MacHugh DE, Park SD, Scraggs E, Haley CS, Lynn DJ, Boland MP, Doherty ML. Linkage mapping of the locus for inherited ovine arthrogryposis (IOA) to sheep chromosome 5. Mamm Genome. 2007 Jan; 18(1):43-52.
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