The significance of pathological spontaneous activity in various myopathies

被引:15
作者
Hanisch, F. [1 ]
Kronenberger, C. [1 ]
Zierz, S. [1 ]
Kornhuber, M. [1 ]
机构
[1] Univ Halle Wittenberg, Dept Neurol, D-06120 Halle, Saale, Germany
关键词
Complex repetitive discharges; Myotonic discharges; Electromyography; Limb girdle muscular dystrophy; Matrin; 3; myopathy; FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY; INCLUSION-BODY MYOSITIS; CENTRONUCLEAR MYOPATHY; MYOTONIC DISCHARGES; POMPE-DISEASE; CLINICAL SPECTRUM; DYNAMIN; DYSFERLINOPATHY; MUTATIONS; PHENOTYPE;
D O I
10.1016/j.clinph.2013.11.021
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Pathological spontaneous activity (PSA) in electromyography (EMG) has not yet been systematically analysed in various types of myopathies. Methods: 136 Patients with well-defined myopathies were retrospectively analysed for the presence of PSA in distal, proximal, and paravertebral muscles. PSA comprised fibrillations (fib)/positive sharp waves (PSW) and high frequency discharges (HFD; i.e., myotonic and complex repetitive discharges). Results: fib/PSW occurred more frequently than HFD. HFD were rarely myotonic in nature. 50% and more patients presented with HFD in PROMM (80%), Pompe's disease (70%), matrin-3 myopathy (60%), sIBM (50%), CNM (50%), while far less than 50% of the patients showed RD in LGMD2I (21%), LGMD2A (17%), LGMD2B (17%), LGMD2L (14%), FSHD (4%), BMD (0%). Four different HFD patterns were proposed. Conclusion: The segregation of myopathies relative to the occurrence of PSA and especially HFD in a high prevalence group and in a low prevalence group may be diagnostically valuable. Significance: The screening for HFD by means of EMG is also valuable in the diagnosis of non-myotonic myopathies. (C) 2013 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1485 / 1490
页数:6
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