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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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".

Diseases [C]
Musculoskeletal Diseases [C05]
Joint Diseases [C05.550]
Arthrogryposis [C05.550.150]
Muscular Diseases [C05.651]
Arthrogryposis [C05.651.102]
Musculoskeletal Abnormalities [C05.660]
Arthrogryposis [C05.660.077]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Musculoskeletal Abnormalities [C16.131.621]
Arthrogryposis [C16.131.621.077]

Below are MeSH descriptors whose meaning is related to "Arthrogryposis".

Below are MeSH descriptors whose meaning is more specific than "Arthrogryposis".

publications

Timeline | Most Recent

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.

Bar chart showing 42 publications over 16 distinct years, with a maximum of 7 publications in 2017 and 2019

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1996	1	0	1
2006	1	0	1
2007	1	0	1
2008	1	0	1
2009	2	0	2
2012	2	0	2
2013	1	0	1
2014	1	1	2
2015	2	0	2
2017	7	0	7
2018	1	0	1
2019	7	0	7
2020	3	0	3
2021	2	0	2
2022	3	0	3
2024	5	1	6

Below are the most recent publications written about "Arthrogryposis" by people in Profiles.

Nematollahi S, Rampakakis E, Amara M, Hamdy RC, Rauch F, Hyer LC, James MA, Altiok H, Raney E, Pellett J, Mielke C, Nossov SB, Tavukcu S, Giampietro PF, Dahan-Oliel N. Health-related quality of life in 205 children with arthrogryposis multiplex congenita. Qual Life Res. 2025 Jan; 34(1):247-260.

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Rice SM, Varotsis DF, Wodoslawsky S, Critchlow E, Liu R, McLaren RA, Makhamreh MM, Firman B, Berger SI, Al-Kouatly HB. Prenatal Phenotype of Alkuraya-Kucinskas Syndrome: A?Novel Case and Systematic Literature Review. Prenat Diagn. 2024 10; 44(11):1381-1397.

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Nematollahi S, Dieterich K, Filges I, De Vries JIP, Van Bosse H, Natera-De Benito D, Hall JG, Sawatzky B, Bedard T, Sanchez VC, Navalon-Martinez C, Pan T, Hilton C, Dahan-Oliel N. ?l?ments de donn?es communs pour l'arthrogrypose multiple cong?nitale: Un cadre international. Dev Med Child Neurol. 2024 Oct; 66(10):e200-e207.

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Nematollahi S, Dieterich K, Filges I, De Vries JIP, Van Bosse H, Natera de Benito D, Hall JG, Sawatzky B, Bedard T, Sanchez VC, Navalon-Martinez C, Pan T, Hilton C, Dahan-Oliel N. Elementos de datos comunes para la artrogriposis m?ltiple cong?nita: Un marco internacional. Dev Med Child Neurol. 2024 Oct; 66(10):e192-e199.

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Lemin S, van Bosse HJP, Hutka L, Soberdash S, Patibandla J. Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey. Prenat Diagn. 2024 05; 44(5):614-622.

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Nematollahi S, Dieterich K, Filges I, De Vries JIP, Van Bosse H, Natera de Benito D, Hall JG, Sawatzky B, Bedard T, Sanchez VC, Navalon-Martinez C, Pan T, Hilton C, Dahan-Oliel N. Common data elements for arthrogryposis multiplex congenita: An international framework. Dev Med Child Neurol. 2024 Oct; 66(10):1340-1347.

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Dahan-Oliel N, van Bosse H, Darsaklis VB, Rauch F, Bedard T, Bardai G, James M, Raney E, Freese K, Hyer L, Altiok H, Pellett J, Giampietro P, Hall J, Hamdy RC. 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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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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Latypova X, Creadore SG, Dahan-Oliel N, Gustafson AG, Wei-Hung Hwang S, Bedard T, Shazand K, van Bosse HJP, Giampietro PF, Dieterich K. A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita. Genes (Basel). 2021 07 08; 12(7).

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