Medikal Retina
Derleme
Printed Date: 26.11.2018
Genetic and Risk Factors in Central Retinal Venous Occlusion with Macular Edema
Abstract
Retinal venous occlusions are the most common cause of blindness after diabetic retinopathy. Incidence of the disease increases with the age. There are systemic, genetic, and ocular risk factors that set the backround of disease. Methyltetrahydrofolate reductase (MTHFR) enzyme gene mutation (MTHFR C677T) increases the plasma levels of homocysteine and the thrombosis tendency. Factor V Leiden polymorphism FVR506Q, prothrombin (FII) G20210A, angiotensin converting enzyme (ACE) ins287del and angiotensinogen (AGT) T235M are other common gene mutations for thromboembolic events. Systemic risk factors such as hypertension, hyperlipidemia, cigarette smoking, diabetes mellitus and obesity are the diseases which make atherosclerosis. Other ocular risk factors are glaucoma, orbital masses with inflammation and glob trauma.
Keywords: Hyperhomocysteinemia, hypertension, genetic, risk factors, central retinal vein occlusion
. . .
Article Information
Received : 31.05.2018
Accepted : 26.11.2018
First Published (online): 26.11.2018
Printed : 1.01.2019
Accepted : 26.11.2018
First Published (online): 26.11.2018
Printed : 1.01.2019
Citation : Akay F, Altınışık M, Güven Ziya Y. Santral Retinal Ven Tıkanıklığı ile Maküla Ödeminde Genetik ve Risk Faktörleri, Güncel Retina 2019;3(1): 5-8.