Alexander K R, Fishman G A
Br J Ophthalmol. 1984 Feb;68(2):69-78. doi: 10.1136/bjo.68.2.69.
Three patients with a bull's-eye macular lesion and other signs characteristic of cone dystrophy gave an unusual ERG finding. In response to a white flash of moderate intensity the scotopic b-wave amplitude was considerably larger than normal. One patient had elevated rod thresholds and nyctalopia, while the other 2 had normal rod sensitivity associated with the supernormal scotopic b-wave amplitude. In the latter 2 patients the abnormal ERG pattern was unchanged for 4 years and 7 years respectively. This atypical finding, of a supernormal scotopic b-wave amplitude in response to light of moderate intensity, appears to characterise a subgroup of patients with cone dystrophy, probably of autosomal recessive inheritance. The pathogenesis of the abnormal ERG remains uncertain.
三名患有靶心黄斑病变及其他符合视锥细胞营养不良特征体征的患者出现了异常的视网膜电图(ERG)表现。对于中等强度的白色闪光刺激,暗视b波振幅显著大于正常。其中一名患者杆细胞阈值升高且有夜盲症,而另外两名患者杆细胞敏感性正常,但暗视b波振幅超常。后两名患者的异常ERG模式分别在4年和7年内未发生变化。这种对中等强度光刺激出现超常暗视b波振幅的非典型表现,似乎是视锥细胞营养不良患者中的一个亚组特征,可能为常染色体隐性遗传。异常ERG的发病机制仍不确定。