一例小口氏病合并先天性视网膜劈裂症的病例。
A case of a combination of Oguchi's disease and congenital retinoschisis.
作者信息
Ohguro H, Suzuki J, Nakagawa T
机构信息
Department of Ophthalmology, Sapporo Medical University School of Medicine, Sapporo, Japan.
出版信息
Ophthalmologica. 1998;212(5):347-9. doi: 10.1159/000027323.
PMID:9693296
Abstract
We report here a rare case of a combination of Oguchi's disease and congenital retinoschisis. A 36-year-old male patient presented with a decrease in vision in both eyes and night blindness. Indirect ophthalmoscopy revealed bilateral macular stellate striations and golden-gray discoloration of the retina outside the vascular arcades. This discoloration turned to a normal retina after complete adaptation to darkness (Mizuo-Nakamura phenomenon).
摘要
我们在此报告一例罕见的小柳原田病与先天性视网膜劈裂症合并的病例。一名36岁男性患者出现双眼视力下降及夜盲症状。间接检眼镜检查发现双侧黄斑区有星芒状条纹，血管弓外视网膜呈金灰色变色。在完全适应黑暗后，这种变色转变为正常视网膜（水尾-中村现象）。
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