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一种罕见的疼痛性非萎缩性肌强直形式。

A rare form of painful nondystrophic myotonia.

作者信息

Torbergsen T, Hødnebø A, Brautaset N J, Løseth S, Stålberg E

机构信息

Department of Neurology, Tromsø University Hospital, Tromsø, Norway.

出版信息

Clin Neurophysiol. 2003 Dec;114(12):2347-54. doi: 10.1016/s1388-2457(03)00275-x.

Abstract

OBJECTIVE

In this paper we report a painful nondystrophic myotonia which has not been previously described. Pain is a rare symptom in myotonia. We report a myotonic disorder in a 34-year-old woman and her 14-year-old daughter. Painful cramps occur during and after exercise in the mother, and both patients can demonstrate unusual contractions in the tongue. In the present study we try to evaluate the mechanisms behind the unique finding of trains of high amplitude of positive waves, not seen in the earlier known myotonic conditions.

METHODS

Clinical investigations and electromyography with single and dual channel recordings and muscle morphometry were performed.

RESULTS

The electromyographic recordings reveal positive waves, fibrillation potentials and myotonic discharges. In addition, extraordinary findings were made of trains of high frequency positive potentials with very high amplitudes and with conduction block along the muscle fibres.

CONCLUSIONS

In this new form of myotonia with likely dominant heredity, the specific finding of trains of high amplitude positive waves indicates ephaptic transmission within bundles of neighbouring muscle fibres.

摘要

目的

在本文中,我们报告了一种此前未被描述过的疼痛性非营养不良性肌强直。疼痛在肌强直中是一种罕见症状。我们报告了一名34岁女性及其14岁女儿患有肌强直障碍。母亲在运动期间及运动后会出现疼痛性痉挛,且两名患者的舌头均能表现出异常收缩。在本研究中,我们试图评估在早期已知的肌强直病症中未出现的一连串高振幅正波这一独特发现背后的机制。

方法

进行了临床检查、单通道和双通道记录的肌电图检查以及肌肉形态测量。

结果

肌电图记录显示有正波、纤颤电位和肌强直放电。此外,还发现了一连串高频正电位,其振幅非常高,且沿肌纤维存在传导阻滞,这是异常发现。

结论

在这种可能为显性遗传的新型肌强直中,一连串高振幅正波的特定发现表明相邻肌纤维束内存在ephaptic传递。

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