Thrombophilia: genetic polymorphisms and their association with retinal vascular occlusive disease

Br J Ophthalmol. 2001 Jul;85(7):883-6. doi: 10.1136/bjo.85.7.883.

Authors

M Chak¹, G R Wallace, E M Graham, M R Stanford

Affiliation

¹ Department of Ophthalmology, GKT, St Thomas's Hospital, Lambeth Palace Road, London SE1 7EH, UK.

No abstract available

Publication types

Research Support, Non-U.S. Gov't
Review

MeSH terms

Behcet Syndrome / complications
Factor V / genetics
Humans
Hyperhomocysteinemia / complications
Methylenetetrahydrofolate Reductase (NADPH2)
Oxidoreductases Acting on CH-NH Group Donors / genetics
Polymorphism, Genetic*
Prothrombin / genetics
Retinal Vein Occlusion / etiology
Retinal Vein Occlusion / genetics*
Risk Factors
Thrombophilia / etiology
Thrombophilia / genetics*

Substances

factor V Leiden
Factor V
Prothrombin
Oxidoreductases Acting on CH-NH Group Donors
Methylenetetrahydrofolate Reductase (NADPH2)