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DOI: 10.1055/s-0031-1273239
© Georg Thieme Verlag KG Stuttgart · New York
Importance of Complete Haematological Workup for Relatives of Young Patients presenting Central Retinal Vein Occlusion
Stellenwert einer vollständigen hämatologischen Abklärung bei Familienangehörigen von jungen Patienten mit Zentralvenen-VerschlussPublication History
Publication Date:
11 April 2011 (online)
![](https://www.thieme-connect.de/media/klimo/201104/lookinside/thumbnails/10.1055-s-0031-1273239-1.jpg)
Background
Central retinal vein occlusion is frequently associated with cardiovascular risk factors (arterial hypertension, hypercholesterolemia), or local factors such as ocular hypertension. However, in young patients (under 50), haematological and inflammatory factors (e. g. factor V Leiden, mutation of prothrombin, hypercysteinemia) must be further investigated [1] [2].
We report the case of a young patient presenting with a non-ischemic central retinal vein occlusion associated with a G 20210A mutation and discuss the relevance of this result for her relatives.
References
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- 3 De Stefano V, Martinelli I, Mannucci P M et al.. The risk of reccurent venous thromboembolism among heterozygous carriers of G 20210A prothrombin gene mutation. British Journal of Heamatology. 2001; 113 630-635
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