Harada T, Miyake Y, Natsume K
Ophthalmologica. 1984;188(4):259-65. doi: 10.1159/000309372.
Description of a man with heredoataxia, presenting with an isolated primary atrophic maculopathy in which the participation of the posterior pole was disclosed by photopic and scotopic ERG irrespective of the localized appearance of this condition. Ophthalmoscopically, the patient's sister showed only fine pigment migrations at the macula, whereas local ERG revealed a macular lesion.
一名患有遗传性共济失调的男性病例描述,其表现为孤立性原发性萎缩性黄斑病变,无论该病症的局部外观如何,明视和暗视视网膜电图均显示后极部受累。眼底检查时,患者的妹妹仅在黄斑区有细微的色素迁移,而局部视网膜电图显示有黄斑病变。