论文部分内容阅读
作者通过玻璃体荧光光度测定(VF)研究无脉络膜症和X-连锁遗传性视网膜色素变性(XLRP)携带者的血-视网膜屏障功能的异常,以及血-视网膜屏障功能障碍和ERG波幅降低与视网膜色素改变的关系。研究对象包括10例XLRP携带者(年龄19～55岁,平均41.7岁),其中9例为专性携带者,8例双眼底呈金箔样反光;8例无脉络膜症携带者(年龄12～59岁,平均年龄37.4岁),其中6例是专性携带者,8例眼底均有不同程度的色素斑驳或遍布后极部和中周视网膜的虫蛀状改变。使用带有标准化亮度的Snellen投影图进行视力
The authors studied the abnormality of the blood-retinal barrier function in choroid-free and X-linked inherited retinitis pigmentosa (XLRP) patients by vitreous fluorimetry (VF) and the association between blood-retinal barrier dysfunction and decreased ERG amplitude with retinal pigment Change the relationship. The subjects included 10 XLRP carriers (age 19-55 years, average 41.7 years), 9 of whom were obligate carriers and 8 eyes with gold foil-like reflexes. Eight patients without choroidal asphyxiation (age 12-59 Year-old, average age 37.4 years), of which 6 were obligate carriers, 8 patients with varying degrees of pigmented mottled mottled or around the posterior pole and the middle of the week of the retina worm-like changes. Use Snellen projection with standardized brightness for vision