"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 |
---|
2010 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2019 | 3 | 1 | 4 |
2022 | 2 | 1 | 3 |
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Below are the most recent publications written about "Arthrogryposis" by people in Profiles.
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The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications. Brain. 2022 11 21; 145(11):3816-3831.
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Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis. Genet Med. 2022 10; 24(10):2187-2193.
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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.
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The adult phenotype of Schaaf-Yang syndrome. Orphanet J Rare Dis. 2020 10 19; 15(1):294.
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Arthrogryposis. Am J Obstet Gynecol. 2019 12; 221(6):B7-B9.
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Congenital talipes equinovarus (clubfoot). Am J Obstet Gynecol. 2019 12; 221(6):B10-B12.
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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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The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance. Am J Hum Genet. 2019 07 03; 105(1):132-150.
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Identification of KLHL40 mutations by targeted next-generation sequencing facilitated a prenatal diagnosis in a family with three consecutive affected fetuses with fetal akinesia deformation sequence. Prenat Diagn. 2016 Dec; 36(12):1135-1138.
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Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin. J Clin Invest. 2016 Feb; 126(2):762-78.