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遗传性黄斑变性在视网膜病变中,并非罕见,临床上有时常被忽略,现将结合眼底荧光血管造影的四例,报道如下。病例报告例1 刘×,男性,24岁。1984年12月来我院就诊。主诉青春期时感视力明显减退,无夜盲史。检查:视力,右眼0.03;左眼0.05,不能矫正。双眼眼前节段正常,检眼镜检查:视乳头正常,视网膜血管略较正常为细,黄斑区可见横椭园形的金箔样反光区,病变区横径右眼为1.5PD,左眼为1 PD,反光区内散在色素点,中心凹反射消
Hereditary macular degeneration in retinopathy, is not uncommon, sometimes clinically often overlooked, now combined with fundus fluorescein angiography in four cases reported below. Case Report 1 Liu ×, male, 24 years old. 1984 December to our hospital. Appear puberty significantly decreased visual acuity, no night blindness. Check: visual acuity, right eye 0.03; left eye 0.05, can not be corrected. Eyes before the segment normal, ophthalmoscopy: normal papillae, retinal blood vessels slightly more than normal, the macular area can be seen horizontal oval-shaped gold foil-like reflective area, the lesion diameter of the right eye is 1.5PD, the left eye is 1 PD , Reflective area scattered in the pigment point, foveal reflection elimination