"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 3 | 0 | 3 |
| 2022 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Arthrogryposis" by people in Profiles.
-
Anetumab ravtansine versus vinorelbine in patients with relapsed, mesothelin-positive malignant pleural mesothelioma (ARCS-M): a randomised, open-label phase 2 trial. Lancet Oncol. 2022 04; 23(4):540-552.
-
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis. Am J Hum Genet. 2019 10 03; 105(4):689-705.
-
Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence. Exp Neurol. 2019 10; 320:112961.
-
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.
-
Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria. Neuromuscul Disord. 2016 11; 26(11):744-748.
-
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.
-
Mutation of perinatal myosin heavy chain associated with a Carney complex variant. N Engl J Med. 2004 Jul 29; 351(5):460-9.
-
Arthrogryposis multiplex congenita with Peter's anomaly. J Pediatr Ophthalmol Strabismus. 1990 Nov-Dec; 27(6):329.