Lepore F E, Duvoisin R C
Neurology. 1985 Mar;35(3):423-7. doi: 10.1212/wnl.35.3.423.
Apraxia of lid opening was described by Goldstein and Cogan as "a non paralytic motor abnormality characterized by the patient's difficulty in initiating the act of lid elevation." We studied six such patients with this finding accompanied by vigorous frontalis contraction and no evidence of ongoing orbicularis oculi contraction, dysfunction of the oculomotor nerve, or loss of ocular sympathetic innervation. Four patients had Parkinson's disease or atypical parkinsonism, one had progressive supranuclear palsy, and one had Shy-Drager syndrome. At onset of ocular symptoms, mean age was 64 years, and the mean duration of extrapyramidal symptoms was 9.7 years. By definition, the motor system must be intact in any apraxia. Therefore, this disorder of lid opening in patients with extrapyramidal motor dysfunction is not an apraxia, but rather involuntary levator palpebrae inhibition of supranuclear origin.
戈德斯坦和科根将眼睑开合失用描述为“一种非麻痹性运动异常,其特征是患者在开始眼睑上抬动作时存在困难”。我们研究了6例有此表现的患者,其伴有额肌强力收缩,且没有眼轮匝肌持续收缩、动眼神经功能障碍或眼交感神经支配丧失的证据。4例患者患有帕金森病或非典型帕金森综合征,1例患有进行性核上性麻痹,1例患有夏伊-德雷格综合征。出现眼部症状时的平均年龄为64岁,锥体外系症状的平均持续时间为9.7年。根据定义,在任何失用症中运动系统必须完整。因此,锥体外系运动功能障碍患者的这种眼睑开合障碍并非失用症,而是源于核上的提上睑肌非自主性抑制。