Shaibani Aziz
Department of Medicine, Nerve and Muscle Center of Texas, Baylor College of Medicine, 6624 Fannin # 1670, Houston, TX 77030, USA.
Neurol Clin. 2016 Aug;34(3):547-64. doi: 10.1016/j.ncl.2016.04.014.
About 15% of myopathies present with distal weakness. Lack of sensory deficit, and preservation of sensory responses and deep tendon reflexes, favors a myopathic cause for distal weakness. Electromyogram confirms this diagnosis. Profuse spontaneous discharges are common in inflammatory, metabolic, and myofibrillar myopathy (MFM). If the clinical picture indicates a specific disease such as facioscapulohumeral muscular dystrophy (FSHD), genetic testing provides the quickest diagnosis. Otherwise, muscle biopsy can distinguish specific features. The common causes of myopathic distal weakness are FSHD, myotonic dystrophy, and inclusion body myositis. Other causes include MFM, distal muscular dystrophies, metabolic myopathies, and congenital myopathies.
约15%的肌病表现为远端肌无力。无感觉缺失、感觉反应及深腱反射保留,提示远端肌无力的病因是肌病。肌电图可确诊。大量自发电活动在炎性、代谢性和肌原纤维肌病(MFM)中很常见。如果临床表现提示某种特定疾病,如面肩肱型肌营养不良症(FSHD),基因检测可提供最快的诊断。否则,肌肉活检可区分特定特征。肌病性远端肌无力的常见病因是FSHD、强直性肌营养不良症和包涵体肌炎。其他病因包括MFM、远端型肌营养不良症、代谢性肌病和先天性肌病。