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Medical Definition of Arthrogryposis multiplex congenita
1. Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000)
Lexicographical Neighbors of Arthrogryposis Multiplex Congenita
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