Arthrogryposis Multiplex Congenita
朴康姬, 吳貞姬,
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朴康姬 ( )
高麗大學校 醫科大學 再活醫學敎室
吳貞姬 ( )
高麗大學校 醫科大學 再活醫學敎室
KMID : 0361419770010020077
Abstract
Arthrogryposis Multiplex Congenita Is a very rare :disease which .present at birth and non :progress in character.
This disorder is characterized by limitation of motion of the joints . of the :extremities involved and appearance of marked wasting, due to diminished muscle substance, -increased fibrous tissue about the joints, distrbance of joint mobility, and characteristic deformity.
This paper reports one case of arthrogryposis. The characteristic clinical aspects of joint deformities, laboratory and :electromyographic findings are presented with a review of literature.
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