Smolenski C, Ludin H P
Fortschr Neurol Psychiatr. 1984 Jun;52(6):215-21. doi: 10.1055/s-2007-1002020.
In five members belonging to a Swiss kinship the typical signs of Roussy-Levy's syndrome are described, such as disturbances of gait and of standing, areflexia, foot deformities, slight muscular weakness and atrophies, minimal sensory disturbances and the typical course of the disease. The patients have been examined electrophysiologically and disturbances of sensory conduction velocity and sensory nerve action potentials are described. The question whether Roussy-Lévy's syndrome represents a disease entity or not, is discussed. The authors feel that the syndrome belongs to HMSN type I.
本文描述了瑞士一个家族中五名成员的罗西-莱维综合征典型症状，如步态和站立障碍、无反射、足部畸形、轻微肌肉无力和萎缩、轻微感觉障碍以及该疾病的典型病程。对患者进行了电生理检查，并描述了感觉传导速度和感觉神经动作电位的障碍。文中讨论了罗西-莱维综合征是否为一种独立疾病的问题。作者认为该综合征属于遗传性运动感觉神经病I型。
