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Anti-MuSK-Positive Myasthenia Gravis in a Patient with Parkinsonism and Cognitive Impairment

机译:帕金森氏症和认知障碍患者的抗Mus阳性重症肌无力

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Muscle-specific tyrosine kinase- (MuSK-) antibodies-positive Myasthenia Gravis accounts for about one third of Seronegative Myasthenia Gravis and is clinically characterized by early onset of prominent bulbar, neck, shoulder girdle, and respiratory weakness. The response to medical therapy is generally poor. Here we report a case of late-onset MuSK-antibodies-positive Myasthenia Gravis presenting with signs of cognitive impairment and parkinsonism in addition to bulbar involvement and external ophthalmoplegia. The pattern of involvement of both peripheral and central nervous system dysfunction might suggest a common pathogenic mechanism, involving impaired cholinergic transmission.
机译:肌肉特异性酪氨酸激酶(MuSK-)抗体阳性的重症肌无力约占血清阴性的重症肌无力的三分之一,临床特征是明显的延髓,颈部,肩带和呼吸系统无力。对药物治疗的反应通常较差。在这里,我们报告一例迟发性MuSK抗体阳性的重症肌无力,除了延髓受累和外部眼肌麻痹外,还伴有认知障碍和帕金森氏症的迹象。周围和中枢神经系统功能障碍的累及模式可能提示一种常见的致病机制,涉及胆碱能传递受损。

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