英语语法分析

Clinical features include microspherophakia, lens ectopia, glaucoma, brachydactyly, short status and so on.

临床表现为球形晶状体、晶状体脱位、青光眼、短指、身材矮小等。

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。