Noble K G, Sherman J
Department of Ophthalmology, New York University Medical Center, NY 10010.
Am J Ophthalmol. 1989 Sep 15;108(3):255-9. doi: 10.1016/0002-9394(89)90115-3.
Three members from two successive generations demonstrated a bilateral, symmetric pigmentary maculopathy consisting of a diffuse yellowish sheen of the posterior pole. The visual acuity was variable (20/25 to 10/400) and visual function tests indicated a localized disorder. Historic information suggests the disorder is slowly progressive. On the basis of mode of inheritance, fundus and angiographic appearance, and visual function testing this appears to be a newly described disorder.
来自连续两代的三名成员表现出双侧对称性色素性黄斑病变，其特征为后极部弥漫性淡黄色光泽。视力各不相同（20/25至10/400），视觉功能测试表明存在局部性病变。既往信息提示该病变呈缓慢进展。根据遗传方式、眼底及血管造影表现以及视觉功能测试，这似乎是一种新描述的疾病。
