"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
|
MeSH Number(s) |
C05.550.150 C05.651.102 C05.660.077 C16.131.621.077
|
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
|
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.
View timeline visualization
Year | Major Topic | Minor Topic | Total |
---|
1997 | 0 | 2 | 2 |
2001 | 1 | 0 | 1 |
2006 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2009 | 3 | 0 | 3 |
2010 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2012 | 2 | 1 | 3 |
2013 | 1 | 0 | 1 |
2014 | 1 | 1 | 2 |
2015 | 4 | 2 | 6 |
2016 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2019 | 6 | 1 | 7 |
2020 | 4 | 0 | 4 |
2022 | 2 | 0 | 2 |
2023 | 1 | 0 | 1 |
2024 | 1 | 1 | 2 |
Below are the most recent publications written about "Arthrogryposis" by people in Profiles.
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Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfecta. J Bone Miner Res. 2024 Sep 02; 39(9):1240-1252.
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Hereditary Neuropathy with Liability to Pressure Palsy and Vocal Cord Paralysis After Pulmonary Lobectomy: A Case Report. A A Pract. 2024 Mar 01; 18(3):e01752.
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Genetic Mechanisms of Migraine: Insights from Monogenic Migraine Mutations. Int J Mol Sci. 2023 Aug 11; 24(16).
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Epidemiology, aetiology, interventions and genomics in children with arthrogryposis multiplex congenita: protocol for a multisite registry. BMJ Open. 2022 10 28; 12(10):e060591.
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Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome. J Thromb Haemost. 2022 07; 20(7):1712-1719.
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Drosophila myosin mutants model the disparate severity of type 1 and type 2B distal arthrogryposis and indicate an enhanced actin affinity mechanism. Skelet Muscle. 2020 08 15; 10(1):24.
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Arthrogryposis Multiplex Congenita. Pediatr Ann. 2020 Jul 01; 49(7):e299-e304.
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A novel pathogenic mutation in the COL7A1 gene resulting in mild autosomal dominant bullous dermolysis of the newborn. Pediatr Dermatol. 2020 Sep; 37(5):955-957.
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Restoration of Elbow Flexion With a Free Functional Gracilis Muscle Transfer in an Arthrogrypotic Patient Using a Motor Nerve to Pectoralis Major. Hand (N Y). 2020 09; 15(5):739-743.
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Comparison of plate and screw constructs versus screws only for anterior distal femoral hemiepiphysiodesis in children. J Pediatr Orthop B. 2020 Jan; 29(1):53-61.