ConclusionThe ARIX gene polymorphisms, especially the nucleotide change of G153A may be one of genetic risk factors for concomitantexotropia.
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。
2
CONCLUSION: Binocular or monocular medial rectus muscle resection in treatment of convergence insufficiency concomitantexotropia 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。
3
Conclusion Muscular lesion of the extraocular muscles of both the master eye and the deviated eye of concomitantexotropia shows no significant difference.