Jampol L M, Sieving P A, Pugh D, Fishman G A, Gilbert H
Arch Ophthalmol. 1984 May;102(5):671-4. doi: 10.1001/archopht.1984.01040030527008.
We examined 11 young patients with unilateral ocular findings that included multiple white dots at the level of the retinal pigment epithelium (RPE) or the deep retina, vitreal cells, RPE granularity in the macula, reduced visual acuity, electroretinogram (ERG) and early receptor potential (ERP) amplitudes, and fluorescein leakage from disc capillaries and late staining of the RPE. Recovery of visual function included a dramatic improvement in ERG and ERP amplitudes over several weeks. The etiology of this syndrome remains uncertain; there is no definite evidence of systemic involvement.
我们检查了11例年轻患者，他们有单侧眼部表现，包括视网膜色素上皮（RPE）或深层视网膜水平的多个白色小点、玻璃体细胞、黄斑区RPE颗粒状改变、视力下降、视网膜电图（ERG）和早期感受器电位（ERP）振幅降低，以及视盘毛细血管荧光素渗漏和RPE晚期染色。视觉功能的恢复包括在数周内ERG和ERP振幅显著改善。该综合征的病因仍不确定；没有明确的全身受累证据。
