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名词信息
中 文 名:
先天性多发关节挛缩症
英 文 名:
congenital multiple arthrogryposis
中文又称:
多发关节挛缩症
中文曾称:
名词来源:
所属专业:
骨科
所属类别:
疾病诊断名词
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Pubmed相关的文献
congenital multiple arthrogryposis
相关文献:
Arthrogryposis Multiplex Congenita.
Langston S, Chu A.
Pediatr Ann. 2020 Jul 1;49(7):e299-e304. doi: 10.3928/19382359-20200624-01.
PMID:32674167
[Congenital multiple arthrogryposis].
Parsch K, Pietrzak S.
Orthopade. 2007 Mar;36(3):281-90; quiz 291. doi: 10.1007/s00132-007-1044-0.
PMID:17323063
Gene ontology analysis of arthrogryposis (multiple congenital contractures).
Kiefer J, Hall JG.
Am J Med Genet C Semin Med Genet. 2019 Sep;181(3):310-326. doi: 10.1002/ajmg.c.31733. Epub 2019 Aug 1.
PMID:31369690
A standardized autopsy protocol for arthrogryposis (multiple congenital contractures).
Oberg KC, Magaki S, Hall JG.
Am J Med Genet C Semin Med Genet. 2019 Sep;181(3):474-478. doi: 10.1002/ajmg.c.31731. Epub 2019 Aug 2.
PMID:31373772
Multiple congenital contractures (congenital multiple arthrogryposis).
Bonilla-Musoles F, Machado LE, Osborne NG.
J Perinat Med. 2002;30(1):99-104. doi: 10.1515/JPM.2002.012.
PMID:11933662
The etiology of arthrogryposis (multiple congenital contracture).
Swinyard CA, Bleck EE.
Clin Orthop Relat Res. 1985 Apr;(194):15-29.
PMID:3884205
Arthrogryposis (multiple congenital contractures): diagnostic approach to etiology, classification, genetics, and general principles.
Hall JG.
Eur J Med Genet. 2014 Aug;57(8):464-72. doi: 10.1016/j.ejmg.2014.03.008. Epub 2014 Apr 3.
PMID:24704792
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J.
J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5.
PMID:33820833
Amyoplasia revisited.
Hall JG, Aldinger KA, Tanaka KI.
Am J Med Genet A. 2014 Mar;164A(3):700-30. doi: 10.1002/ajmg.a.36395. Epub 2014 Jan 23.
PMID:24459070
Arthrogryposis.
Hall JG.
Am Fam Physician. 1989 Jan;39(1):113-9.
PMID:2643273
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