Methods Clinical observation and pedigree analysis were undertaken in a family with ectopia lentis. 方法对单纯性晶状体异位一家系进行临床研究和系谱分析。
Methods The time, inducement, anterior chamber exudate and cortex lentis residue of 13 cases were observed. 方法对13例病人的发病时间、诱因、前房渗出和皮质残留情况进行观察。
Further more, it may prevent caligo lentis induced by compound and ultraviolet rays, and fight against retinal pigment epithelium apoptosis induced by ischemia. It is also able to improve cellular immune function. 阻止化学和紫外线诱导的白内障,对抗缺血诱导的视网膜色素上皮细胞凋亡,亦可改善机体细胞免疫功能。
Novel mutation of fibrillin 1 gene cause ectopia lentis in a Chinese family 原纤维蛋白1基因新突变导致单纯性晶状体异位
Screening and Analysis of Fibrillin-1 Gene ( FBN1) Mutation in a Chinese Family with Isolated Ectopia Lentis and Association Study of Schizophrenia and the Polymorphisms of COMT Gene in a Chinese Han Population 一个中国人单纯性晶状体异位家系FBN1基因突变的研究以及中国汉族精神分裂症与COMT基因多态性的关联性分析