Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference5 articles.
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2. Factor V and antithrombin gene mutations in patients with idiopathic central retinal vein occlusion;Hodgkins;Eye,1995
3. Bilateral retinal vein occlusion associated with 5,10-methylenetetrahydrofolate reductase mutation;Loewenstein;Am J Ophthalmol,1997
4. A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis;Poort;Blood,1996
5. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease;Ferraresi;Arterioscler Thromb Vasc Biol,1997
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1. Update on Retinal Vein Occlusion;Asia-Pacific Journal of Ophthalmology;2023-02-14
2. Une cause rare d’occlusion de la veine centrale de la rétine chez le sujet jeune dans un contexte traumatique;Journal Français d'Ophtalmologie;2012-06
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4. Retinal-Vein Occlusion;New England Journal of Medicine;2010-11-25
5. Retinal vein occlusion: an approach to diagnosis, systemic risk factors and management;Internal Medicine Journal;2008-12
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