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先天性运动和感觉神经病的异质性。

Heterogeneity of congenital motor and sensory neuropathies.

作者信息

Lütschg J, Vassella F, Boltshauser E, Dias K, Meier C

出版信息

Neuropediatrics. 1985 Feb;16(1):33-8. doi: 10.1055/s-2008-1052541.

Abstract

Six children suffering from a congenital motor and sensory neuropathy (CMSN) are described. Severe muscle hypotonia, areflexia and a delay of motor development are detectable in all of them. Sural nerve biopsies exhibited an almost complete absence of myelinated fibres and a correspondingly slow nerve conduction velocity (NCV) of less than 10 m/s was detectable in four patients. A few segments with hypermyelination adjacent to gross hypomyelination were seen in the fifth patient, and the NCV was 15 m/s. The sural nerve of the sixth patient showed a loss of thick myelinated nerve fibres, and his NCV was 25 m/s. These results demonstrate the histological heterogeneity of CMSN which was already detected by the NCV. The relation of our findings to the classification of HMSN by Dyck and Lambert (1968) is discussed.

摘要

本文描述了6例患有先天性运动和感觉神经病(CMSN)的儿童。所有患儿均表现出严重的肌张力减退、无反射以及运动发育迟缓。腓肠神经活检显示,几乎完全缺乏有髓纤维,4例患者的神经传导速度(NCV)相应较慢,低于10m/s。第五例患者在明显的髓鞘形成不足区域附近可见一些节段性髓鞘形成过多,其NCV为15m/s。第六例患者的腓肠神经显示粗大的有髓神经纤维缺失,其NCV为25m/s。这些结果表明,NCV已检测到CMSN在组织学上具有异质性。本文还讨论了我们的研究结果与Dyck和Lambert(1968年)对遗传性运动感觉神经病(HMSN)分类的关系。

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