Serratrice G, Pellissier J F
C.H.U. Timone, Marseille.
Rev Neurol (Paris). 1987;143(12):841-3.
Two further cases of familial brachial plexus syndrome related to a tomacular neuropathy are reported, adding to the ten-odd known cases of this disorder. The principal characteristics are: onset on wakening or during abnormal posture, indolence, recurrences and associated electromyographic features of diffuse neuropathy. These features differentiate this affection from familial forms of shoulder neuralgic amyotrophy.
本文报告了另外两例与轴索性神经病相关的家族性臂丛神经综合征病例,使这种疾病已知病例增加到十多例。主要特征为:睡醒时或异常姿势时起病、病程缓慢、有复发以及伴有弥漫性神经病的肌电图特征。这些特征将本病与家族性肩部神经性肌萎缩区分开来。