先天性多发性关节挛缩症伴神经源性萎缩和短指畸形（作者译）
[Arthogryposis multiplex congenita with neurogenic atrophy and brachydactyly (author's transl)].
作者信息
Eckel U, Spranger J, Klein H
出版信息
Klin Padiatr. 1979 May;191(3):325-9.
PMID:572450
Abstract
Case report of arthrogryposis multiplex congenita with histologically proved neutrogene atrophy of muscles. The also existing reduction deformities of the limbs, showing aplasia and hypoplasia of phalanges may hypothetically be of neuropathic origin.
摘要
先天性多发性关节挛缩症伴组织学证实的中性粒细胞性肌肉萎缩的病例报告。同时存在的肢体复位畸形，表现为指骨发育不全和发育不良，推测可能源于神经性原因。
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