Thrombophilia in Patients with Retinal Vein Occlusion
Multifactorial hereditary thrombophilia was found in patients with retinal vein occlusion in 78.7% of cases, and in 21.3% of cases in combination with lupus anticoagulant (LA). The combination of mutations and polymorphisms in hemostasis genes in patients with retinal vein occlusion (RVO) affects markers of endothelial damage, activating components of the hemostatic system, which clinically manifests as a local thrombohemorrhagic syndrome in the retinal microcirculatory bed.
Authors
- N.Yu. Shishlyannikova
- GV Vavin
- Т.В. Шелковникова
- S.I. Kapustin
- Yu.P. Bessonov
- Kh.P. Takhchidi
Institutions
- Pirogov Russian National Research Medical University (RU)
- Kemerovo State Medical University (RU)
- Kuzbass Institute of Economics and Law (RU)
- National Medical and Surgical Center named after N.I. Pirogov (RU)
- Russian Research Institute of Hematology and Transfusiology (RU)
- Kuzbass State Technical University (RU)
Publication Details
- Journal
- Psychosomatic and Integrative Research
- Published
- 2025-12-30
- DOI
- https://doi.org/10.15275/pssr.2025.0404
- Primary Topic
- Blood Coagulation and Thrombosis Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00