Roggenkämper P, Velho-Groneberg P
Klin Monbl Augenheilkd. 1981 Nov;179(5):357-8. doi: 10.1055/s-2008-1057330.
Case report on a patient with varying motility disturbances. He first presented with typical clinical and electromyographic symptoms and signs of ocular myositis, which subsided after immunosuppressive therapy. Three years later he developed ocular myasthenia. The diagnostic procedures (especially electromyography, immunology, differential diagnosis and possible underlying pathomechanisms are discussed.
一名患有不同运动障碍的患者的病例报告。他最初表现出典型的眼肌炎临床和肌电图症状及体征,经免疫抑制治疗后症状消退。三年后,他患上了眼肌型重症肌无力。文中讨论了诊断程序(尤其是肌电图、免疫学、鉴别诊断及可能的潜在发病机制)。