Serratrice G, Gastaut J L, Pellissier J F
Rev Neurol (Paris). 1978 Nov;134(11):673-84.
A case of distal amyotrophia is reported, in which there was associated isolated clinical and electrical myotonia. Nerve conduction rates were very reduced. The nerves showed rarefaction of nerve fibers with segmentary demyelinization and the formation of bulbar swellings. The signification of this observation is discussed, and it would not appear to be related to peripheral nerve lesions of the type sometimes seen in Steinert's disease or from an association of this affection with Charcot-Marie's disease. It would seem more reasonable to suggest the hypothesis of a particular type of association of a peroneal hypertrophic neuropathy and a myotonia similar to certain cases reported in the published literature.
报告了一例远端肌萎缩症病例,该病例伴有孤立的临床和电肌强直。神经传导速度显著降低。神经显示神经纤维稀疏,节段性脱髓鞘,并形成球样肿胀。讨论了这一观察结果的意义,它似乎与斯坦纳特病中有时可见的那种周围神经病变无关,也与这种疾病与夏科-马里病的关联无关。提出腓骨肥厚性神经病与一种类似于已发表文献中报道的某些病例的肌强直的特定类型关联的假设似乎更合理。