Central retinal artery occlusion associated with the G20210A prothrombin gene (F2) mutation: A case report.

Medicine & Life Sciences

1. Retinal Artery Occlusion 100%
2. Prothrombin 76%
3. Amaurosis Fugax 54%
4. Scleritis 37%
5. Eye 30%
6. Genes 26%
7. Mutation 13%
8. Ischemia 12%
9. Blood Vessels 11%
10. Differential Diagnosis 10%
11. Hyperprothrombinemia 10%
12. apixaban 9%
13. Genetic Variation 9%
14. Visual Acuity 8%
15. Retinal Vessels 8%
16. Metabolic Diseases 7%
17. Anticoagulants 6%
18. Ethics Committees 6%
19. Ocular Vision 5%
20. Perfusion 5%
21. Referral and Consultation 5%
22. Embolism 5%