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Klin Monbl Augenheilkd
DOI: 10.1055/a-2730-1136
DOI: 10.1055/a-2730-1136
Der interessante Fall
Recurrent Vitreous Haemorrhage Due to Atypical Branch Retinal Vein Occlusion in a Patient with HLA-B51 Positivity and Heterozygous PAI-1 4G/5G Polymorphism
Rezidivierende Glaskörperblutung aufgrund atypischer Venenastthrombose bei HLA-B51-Positivität und heterozygotem PAI-1-4G/5G-PolymorphismusAuthors
Background
Branch retinal vein occlusion (BRVO) is a common retinal vascular disorder typically associated with systemic risk factors such as hypertension, diabetes mellitus, or hyperlipidaemia. In atypical or recurrent cases in younger patients, less common aetiologies, including genetic or inflammatory factors, must be considered [1].
Publication History
Received: 24 August 2025
Accepted: 20 October 2025
Article published online:
02 December 2025
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References
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- 2 Bucan K, Plestina Borjan I, Bucan I. et al. Genetic Background of a Recurrent Unusual Combined Form of Retinal Vein Occlusion: A Case Report. Case Rep Ophthalmol 2018; 9: 248-253
- 3 Gori AM, Marcucci R, Fatini C. et al. Impaired fibrinolysis in retinal vein occlusion: a role for genetic determinants of PAI-1 levels. Thromb Haemost 2004; 92: 54-60
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- 5 Russo PD, Damante G, Pasca S. et al. Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control study. Clin Appl Thromb Hemost 2015; 21: 373-377
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- 7 Ji KB, Hu Z, Zhang QL. et al. Retinal microvasculature features in patients with Behcetʼs disease: a systematic review and meta-analysis. Sci Rep 2022; 12: 752
