Ho P C, Feman S S
Ann Ophthalmol. 1981 Aug;13(8):949-51.
A 16-year-old boy with Fabry's disease had sudden onset of diplopia unassociated with any other neurologic symptoms. A right internuclear ophthalmoplegia characterized by optokinetic phenomena and ocular dysmetria was demonstrated. The diplopia resolved spontaneously in six weeks. This is the first reported case of internuclear ophthalmoplegia occurring with Fabry's disease and represents one of the youngest patients to have unilateral internuclear ophthalmoplegia presumably caused by vascular occlusive disease.
一名患有法布里病的16岁男孩突然出现复视，无任何其他神经系统症状。检查发现存在以视动现象和眼球运动失调为特征的右侧核间性眼肌麻痹。复视在六周内自行缓解。这是首例报道的与法布里病相关的核间性眼肌麻痹病例，也是据推测由血管闭塞性疾病导致单侧核间性眼肌麻痹的最年轻患者之一。
