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首页> 外文期刊>Electromyography and Clinical Neurophysiology: International Bimonthly Review >Electromyographic pattern in Duchenne and Becker muscular dystrophy. Part II. Electromyographic pattern in Becker muscular dystrophy in comparison with Duchenne muscular dystrophy.
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Electromyographic pattern in Duchenne and Becker muscular dystrophy. Part II. Electromyographic pattern in Becker muscular dystrophy in comparison with Duchenne muscular dystrophy.

机译:Duchenne和Becker肌营养不良症的肌电图模式。第二部分与杜氏肌营养不良症相比,贝克尔肌营养不良症的肌电图模式。

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BACKGROUND: The aim of this study was to compare the electromyographic pattern in Becker muscular dystrophy (BMD) with that found in Duchenne muscular dystrophy (DMD). MATERIAL AND METHOD: Fourteen men with BMD and 51 boys with DMD were investigated. Proximal muscles were examined: m. biceps brachii (BB) and m. rectus femoris (RF). They were divided according to the clinical criteria in two groups: of those with slight changes (group AB) and of those with severe abnormalities (CD). As in the Part I of the paper our own method of Functional-QEMG was applied in the CNEMG examination. RESULTS AND CONCLUSIONS: Spontaneous activity (fibrillations, complex repetitive discharges) was equally frequent in BMD and DMD. Linked potentials were rather frequent in either group. Myopathic features such as MUAPs low amplitude and area, polyphasic shape were seen in either condition, but more marked in DMD than in BMD. Evaluation of IP recordings revealed that IP amplitude (amplitude size) is low in DMD already at the early stage of lesion but normal or only slightly diminished in BMD. It might perhaps suggest different degrees of lesion in type II MUs between the compared types of muscular dystrophy.
机译:背景:这项研究的目的是比较在贝克尔肌营养不良症(BMD)和在杜兴肌营养不良症(DMD)中发现的肌电图模式。材料与方法:调查了14名BMD男性和51名DMD男孩。检查近端肌肉:m。肱二头肌(BB)和m。股直肌(RF)。根据临床标准将其分为两组:轻度改变(AB组)和重度异常(CD)组。与本文的第一部分一样,我们自己的功能性QEMG方法也被应用到CNEMG检查中。结果与结论:BMD和DMD的自发活动(纤颤,复杂的重复性放电)同样频繁。两组中潜在的联系潜力都相当高。在任何一种情况下都可以看到肌无力特征,例如MUAP低振幅和低面积,多相形状,但DMD中的特征比BMD中的明显。 IP记录的评估表明,在病变早期,DMD中的IP振幅(振幅大小)已经很低,但BMD正常或仅略有下降。可能表明在比较类型的肌肉营养不良之间,II型MU的病变程度不同。

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