Arthrogryposis multiplex congenita: Etiology, genetics, classification, diagnostic approach, and general aspects

被引:193
|
作者
Hall, JG [1 ]
机构
[1] UNIV BRITISH COLUMBIA, DEPT PEDIAT, VANCOUVER, BC V6T 1W5, CANADA
来源
关键词
arthrogryposis; fetal akinesia; joint contractures; amyoplasia; sporadic; genes;
D O I
10.1097/01202412-199707000-00002
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Arthrogryposis is a sign associated with many specific conditions and syndromes. It is a term used to describe the presence of multiple joint contractures that are present at birth. It can be seen in isolation or in association with other congenital abnormalities as part of a syndrome with or without central nervous system involvement. The exact pathogenesis of arthrogryposis is unknown, but all involve fetal akinesia (decreased fetal movement) with subsequent joint contractures. In this article I describe the causes, genetic aspects, classification, and approach to diagnosis.
引用
收藏
页码:159 / 166
页数:8
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