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Article

[Recurrent incomplete central retinal vein occlusion in a patient with hereditary thrombophilia].

Acta medica Croatica : casopis Hravatske akademije medicinskih znanosti - 1 Jan 2006

Duić Jasna, Gverić-Krecak Velka

Abstract excerpt

The aim of the study was to investigate the cause of recurrent monolateral incomplete central retinal vein occlusion in a 44-year-old woman and the association between retinal vein occlusion and factor V Leiden. Cardiovascular studies, color Doppler of the carotids, complete blood analyses, with immunoserology and coagulation tests were performed. Factor V:R 506Q and prothrombin 20210G/A mutation were tested by...

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Source

Identifiers

PMID: 16848214

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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