Slusher M M, Hutton W E
Am J Ophthalmol. 1979 Feb;87(2):152-6. doi: 10.1016/0002-9394(79)90134-x.
At age 26 years a woman who had been blind in the left eye from birth had visual acuity of R.E.: 6/18 (20/60); L.E.: 6/120 (20/400), with 40 prism diopters of left exotropia. The left eye showed a decreased anteroposterior diameter of the globe and a complete retinal detachment behind a cataractous lens. The right eye had a posterior subcapsular lens opacity severe vitreous fibrosis, dragging of the optic disk, and intraretinal and subretinal exudation with a fibrovascular mass in the temporal retina. The patient's 3-year-old daughter had 45 to 50 prism diopters of exotropia, a pendular nystagmus with intraretinal and subretinal dragging of each disk, and early degeneration and band formation in the periphery of each fundus.
一名26岁女性,左眼自幼失明,右眼视力为6/18(20/60),左眼视力为6/120(20/400),伴有40棱镜度的左眼外斜视。左眼眼球前后径减小,白内障晶状体后方有完全性视网膜脱离。右眼有后囊下晶状体混浊、严重的玻璃体纤维化、视盘牵拉、视网膜内和视网膜下渗出,颞侧视网膜有纤维血管团。患者3岁的女儿有45至50棱镜度的外斜视、摆动性眼球震颤,每个视盘有视网膜内和视网膜下牵拉,每个眼底周边早期出现变性和条索形成。