Objective to identify the mutation gene of a Chinese family with ectopia lentis.
目的研究我国单纯性晶状体异位家系的致病基因，并确定基因突变。
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。
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。
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