Mori M, Kuwabara S, Fukutake T, Yuki N, Hattori T
Department of Neurology, Chiba University School of Medicine, Chiba, Japan.
Neurology. 2001 Apr 24;56(8):1104-6. doi: 10.1212/wnl.56.8.1104.
The authors reviewed the clinical features and outcome of Miller Fisher syndrome (MFS) for 50 consecutive patients with MFS including 28 patients who received no immunotherapy. Besides the characteristic clinical triad (ophthalmoplegia, ataxia, and areflexia), pupillary abnormalities, blepharoptosis, and facial palsy are frequent in MFS, whereas sensory loss is unusual despite the presence of profound ataxia. Patients with MFS usually had good recovery and no residual deficits.
作者回顾了50例连续的米勒-费雪综合征（MFS）患者的临床特征和预后，其中28例未接受免疫治疗。除了典型的临床三联征（眼肌麻痹、共济失调和无反射）外，瞳孔异常、上睑下垂和面瘫在MFS中也很常见，而尽管存在严重共济失调，但感觉丧失并不常见。MFS患者通常恢复良好，无残留缺陷。
