Tackmann W
Neurologische Abteilung, Weserbergland-Klinik, Höxter.
Schweiz Rundsch Med Prax. 1992 Dec 15;81(51):1534-7.
Progressive supranuclear palsy, first described as clinical entity by Steele, Richardson and Olszewski, is a degenerative disorder of the central nervous system. Besides progressive supranuclear oculomotor disturbances, other characteristic signs are pseudobulbar paresis, axial rigidity, gait disturbances and subcortical dementia. Misinterpretation in the early stage as Parkinson's disease is frequently seen. A causal therapy is still missing.
进行性核上性麻痹最早由斯蒂尔、理查森和奥尔谢夫斯基作为一种临床实体进行描述,是一种中枢神经系统的退行性疾病。除了进行性核上性动眼神经障碍外,其他特征性体征包括假性球麻痹、轴性强直、步态障碍和皮质下痴呆。早期常被误诊为帕金森病。目前仍缺乏病因治疗方法。