本病系一种原因不明的神经系统综合病征,起病多为急性或亚急性,主要临床表现为两侧肢体对称性不全或完全软瘫,可伴发颅神经及呼吸吞咽障碍,亦可有轻度主观或客观的感觉障碍,并以脑脊液蛋白细胞分离为其特点。国内从1949—1960年报告过51例。现将兰州医学院神经科从1955—1961年32例住院病人之临床观察结合国内文献作一综合分析。 The disease is an unknown cause of the neurological syndrome, most of the onset of acute or subacute, the main clinical manifestations of bilateral limb symmetry incomplete or completely soft, may be associated with cranial nerves and respiratory dysphagia, may also have Mild subjective or objective sensory disturbance, and to the separation of cerebrospinal fluid protein cells as its characteristics. China from 1949 to 1960 reported 51 cases. Now Lanzhou Medical College Department of Neurology from 1955-1961 32 cases of in-patient clinical observation combined with domestic literature for a comprehensive analysis.