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先天性晶体缺损甚为罕见,伴有睫状体囊性改变者国内尚未见报道,我院于1987年7月在门诊发现一例特报告如下。 贺××女性,16岁,湖南省人,因双眼视力下降1年余来我院就诊。视力检查右眼0.4J=1,左眼0.4J=2,眼前段及小瞳眼底检查均属正常,初步诊断为双眼屈光不正。以2％后马托品扩瞳验光,右眼以-1.00球联合-0.50柱×180°轴矫正后视力达1.5,而左眼发现其鼻侧晶体赤道部为近似弓形(约从6点到11点钟方位),除弓形的中部有数条悬韧带外,弓的上、下部均无悬韧带,其对应部位的睫状体膨大向玻璃体腔在10、
Congenital crystal defects are rare, associated with ciliary body cystic changes have not been reported in China, our hospital in July 1987 in the clinic found a special report is as follows. He × × female, 16 years old, Hunan Province, due to binocular vision decreased more than 1 year to our hospital. Right eye examination 0.4J = 1 right eye, left eye 0.4J = 2, anterior segment and pupil fundus examination are normal, the initial diagnosis of binocular refractive error. After 2% of the horsetail dilated optometry, the right eye to -1.00 ball joint -0.50 column × 180 ° axial corrected visual acuity of 1.5, while the left eye found that the nasal optic equator is approximately arched (about 6:00 to 11 o’clock position), in addition to the central arch has several suspensory ligaments, the bow on the lower part of the suspensory ligament, the corresponding parts of the ciliary body enlargement to the vitreous cavity at 10,