1) postoperative membr ane cataract
膜性后发性白内障
2) after-cataract
后发性白内障
1.
Nd:YAG laser posterior capsulotomy for after-cataract;
Nd:YAG激光后囊膜切开术治疗后发性白内障
2.
Uveitis and after-cataract after phacoemulification;
超声乳化白内障术后葡萄膜炎反应与后发性白内障
3.
Prevention of after-cataract in children with intraocular implanted lens captured by the posterior capsule after cataract surgery;
后囊膜人工晶状体夹持法防治儿童后发性白内障28例
3) posterior capsular opacification
后发性白内障
1.
Use of IL-1ra-chitosan drug delivery system in preventing posterior capsular opacification in rabbits;
IL-1ra-壳聚糖缓释剂对兔后发性白内障的抑制作用
2.
Histopathological analysis of posterior capsular opacification formation by different surgical methods on congenital cataract children;
儿童先天性白内障不同术式后发性白内障形成的病理学分析
3.
Evaluation of computerized image analysis system for quantification of posterior capsular opacification;
后发性白内障计算机图像定量分析系统建立与评价(英文)
4) after cataract
后发性白内障
1.
Influence of posterior continuous curvilinear capsulorhexis with or without anterior vitrectomy on after cataract in children:a systematic review;
后囊膜连续环形撕囊联合或不联合前部玻璃体切除对儿童后发性白内障影响的Meta分析
2.
Experimental study on the IL-1ra restrain after cataract in rabbit;
IL-1ra抑制兔后发性白内障的实验研究
3.
Experimental study on prevention of the after cataract by heparin drug delivery system;
肝素缓释系统预防兔后发性白内障
5) Posterior capsule opacification
后发性白内障
1.
Research advances in posterior capsule opacification;
后发性白内障的研究进展
2.
Researches of the prevention and treatment of posterior capsule opacification;
后发性白内障防治的研究
3.
Prospect and current study status of mechanism and medication in posterior capsule opacification;
后发性白内障的发病机制和药物防治的研究现状及前景
6) membranous cataract
膜性白内障
1.
Mutation of 22q11.2-q12.1 gene in a family with autosomal dominant congenital membranous cataract
先天性膜性白内障一家系致病基因的遗传分析
2.
Purpose:To identify the genetic defect in a family with dust- nuclear cataract combined with high myopia and a family with autosomal dominant congenital membranous cataract.
目的对一个先天性白内障合并高度近视家系和一个先天性膜性白内障家系的致病基因进行初步研究,探讨该家系遗传规律,为进一步寻找这两个家系的致病基因提供依据;为进一步探寻先天性白内障遗传规律,建立基因型-表型间联系提供参考。
补充资料：家族性阵发性运动诱发性舞蹈手足徐动症
家族性阵发性运动诱发性舞蹈手足徐动症
亦称“周期性肌张力不全”。系阵发性肌张力不全性舞蹈手足徐动症的一种类型。可为散发，或显性遗传。儿童期起病，青春期加频。临床特点是由主动运动而诱发肌张力不全、舞蹈手足徐动、强直。每日可出现数次，无意识障碍，脑电图正常。用小剂量抗癫痫药有较好效果；也有的用左旋多巴有效。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条