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复发性家族性神经病伴压迫性麻痹易感性:两例报告及神经超微结构研究

Recurrent familial neuropathy with liability to pressure palsies: reports of two cases and ultrastructural nerve study.

作者信息

Dubi J, Regli F, Bischoff A, Schneider C, de Crousaz G

出版信息

J Neurol. 1979 Jan 30;220(1):43-55. doi: 10.1007/BF00313147.

Abstract

Electrophysiological, histological and ultrastructural studies on two patients (one family) with familial neuropathy and a liability to pressure palsies are reported. There was slowing of nerve conduction velocities and increase of distal latencies of clinically affected and clinically non-affected nerves. These alterations were confirmed by biopsy of the sural nerive which had the characterized signs of the disease. Pathogenetically there seems to be an endogeneous metabolic defect of the Schwann cell to synthetize a normal myelin sheath, which is responsible for the particular susceptibility to mechanical damage.

摘要

报告了对两名患有家族性神经病变且易患压迫性麻痹的患者(一家族)进行的电生理、组织学和超微结构研究。临床受累和未受累神经的神经传导速度减慢,远端潜伏期延长。腓肠神经活检证实了这些改变,其具有该疾病的特征性表现。从发病机制来看,似乎存在施万细胞内源性代谢缺陷,无法合成正常的髓鞘,这导致了对机械损伤的特殊易感性。

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