Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T
Arch Ophthalmol. 1986 Jul;104(7):1013-20. doi: 10.1001/archopht.1986.01050190071042.
An analysis of 64 patients with congenital stationary night blindness showed that all had essentially normal fundi. Electroretinography (ERG) showed a normal a wave with extremely reduced b wave (negative type) when recorded with a single bright white stimulus in the dark. We classified these patients into two groups based on the evaluation of rod ERG and/or psychophysical dark adaptation measured with an 11 degree test target at 15 degrees in the upper part of the retina. One group (35 patients) lacked rod function (complete type). Nine patients could not be classified. No pedigree showed a complete and incomplete type in one family. Differences between the two groups in refractive error, photopic function, and oscillatory potentials in the ERG suggest a different pathogenesis. Our analysis may provide a new classification of congenital stationary night blindness with a negative ERG.
对64例先天性静止性夜盲患者的分析表明,所有患者的眼底基本正常。视网膜电图(ERG)显示,在黑暗中用单一明亮白色刺激记录时,a波正常,b波极度降低(阴性型)。我们根据对视网膜上部15度处11度测试目标测量的视杆细胞ERG和/或心理物理学暗适应评估,将这些患者分为两组。一组(35例患者)缺乏视杆细胞功能(完全型)。9例患者无法分类。没有一个家系在一个家族中同时出现完全型和不完全型。两组在屈光不正、明视觉功能和ERG中的振荡电位方面的差异提示发病机制不同。我们的分析可能为ERG阴性的先天性静止性夜盲提供一种新的分类方法。