Berson E L, Simonoff E A
Arch Ophthalmol. 1979 Jul;97(7):1286-91. doi: 10.1001/archopht.1979.01020020028006.
Full-field electroretinograms (ERGs) were recorded after a ten-year interval from four affected patients in a family with dominant retinitis pigmentosa with reduced penetrance; all patients showed decreases in amplitude. Cone ERGs from affected patients (aged 11 to 15 years) in this family as well as from affected patients of comparable ages from two other families with this genetic type, were normal or slightly reduced in amplitude and substantially delayed in b-wave implicit time. In one family, an asymptomatic older patient, representing an apparent skipped generation, showed abnormal full-field cone and rod ERGs that differed in implicit times from those of young affected patients. Evidence is presented to support the idea that the abnormal full-field cone ERGs recorded from young affected patients are due to an abnormal extrafoveal cone contribution to their full-field responses.
对一个显性遗传性视网膜色素变性且外显率降低的家系中的4名患病患者,间隔十年记录了全视野视网膜电图(ERG);所有患者的振幅均降低。该家系中患病患者(年龄在11至15岁之间)以及另外两个具有这种遗传类型的家系中年龄相仿的患病患者的视锥细胞ERG,振幅正常或略有降低,b波潜伏时间显著延迟。在一个家系中,一名无症状的老年患者,代表明显的隔代遗传,其全视野视锥和视杆细胞ERG异常,潜伏时间与年轻患病患者不同。有证据支持这样的观点,即年轻患病患者记录到的异常全视野视锥细胞ERG是由于其全视野反应中外侧膝状体视锥细胞的异常贡献所致。