ConclusionThe ARIX gene polymorphisms, especially the nucleotide change of G153A may be one of genetic risk factors for concomitant exotropia.
结论ARIX基因多态性，尤其是G153 A核苷酸突变可能是共同性外斜视的遗传风险因子。
CONCLUSION: Binocular or monocular medial rectus muscle resection in treatment of convergence insufficiency concomitant exotropia has satisfactory effect.
结论：对于集合不足型共同性外斜视，行双眼或单眼内直肌缩短术可获得较满意的效果。
Conclusion Muscular lesion of the extraocular muscles of both the master eye and the deviated eye of concomitant exotropia shows no significant difference.
结论共同性外斜视主视眼与主斜眼眼外肌均发生了肌源性病变。
Objective To find out whether there is any difference in extraocular muscles histology between the master eye and the deviated eye of concomitant exotropia.
目的探讨共同性外斜视主视眼与主斜眼眼外肌组织学上有无差异。
Objective To explore the operation curative effect of extra large recession of external rectus in the treatment of concomitant exotropia which amblyopia and allophthalmia.
目的探讨在弱视眼或主斜眼上行外直肌超常量后徙治疗大度数共同性外斜视的手术疗效。
The cycloplegic refractive states of 446 children with concomitant strabismus, including 383 cases of esotropia and 63 exotropia are presented.
本文介绍446例共同性斜视儿童用睫状肌麻痹剂后的屈光状态。446例中，383例为内斜视，63例为外斜视。
The cycloplegic refractive states of 446 children with concomitant strabismus, including 383 cases of esotropia and 63 exotropia are presented.
本文介绍446例共同性斜视儿童用睫状肌麻痹剂后的屈光状态。446例中，383例为内斜视，63例为外斜视。
应用推荐