ARTHROGRYPOSIS MULTIPLEX CONGENITA - ETIOLOGY, GENETICS, CLASSIFICATION, DIAGNOSTIC-APPROACH, AND GENERAL-ASPECTS

Authors
Citation
Jg. Hall, ARTHROGRYPOSIS MULTIPLEX CONGENITA - ETIOLOGY, GENETICS, CLASSIFICATION, DIAGNOSTIC-APPROACH, AND GENERAL-ASPECTS, Journal of pediatric orthopedics. Part B, 6(3), 1997, pp. 159-166
Citations number
36
Categorie Soggetti
Orthopedics,Pediatrics
ISSN journal
1060152X
Volume
6
Issue
3
Year of publication
1997
Part
B
Pages
159 - 166
Database
ISI
SICI code
1060-152X(1997)6:3<159:AMC-EG>2.0.ZU;2-Z
Abstract
Arthrogryposis is a sign associated with many specific conditions and syndromes. It is a term used to describe the presence of multiple join t contractures that are present at birth. It can be seen in isolation or in association with other congenital abnormalities as part of a syn drome with or without central nervous system involvement. The exact pa thogenesis of arthrogryposis is unknown, but all involve fetal akinesi a (decreased fetal movement) with subsequent joint contractures. In th is article I describe the causes, genetic aspects, classification, and approach to diagnosis.