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。
Method The location, intubation pathway, treatment methods and outcomes in 25 cases of PICC ectopia were analyzed retrospectively.
方法通过回顾性分析，对25例PICC异位的发生部位、置管途径、处理方法及结果进行研究、总结。
Once hydrocephalus is ruled out, the degree of tonsillar ectopia and the presence of hydromyelia are evaluated, than the treatment may be performed, based on the indication of clinical symptoms.
一旦排除脑积水，需评价小脑下疝下移程度以及是否出现脊髓积水，基于临床症状可实施治疗。
Once hydrocephalus is ruled out, the degree of tonsillar ectopia and the presence of hydromyelia are evaluated, than the treatment may be performed, based on the indication of clinical symptoms.
一旦排除脑积水，需评价小脑下疝下移程度以及是否出现脊髓积水，基于临床症状可实施治疗。
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