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Article

[Mixed retinal thrombosis in a patient carrying prothrombin gene mutation in a homozygote state].

Journal francais d'ophtalmologie - 1 Nov 1999

Kling F, Macarez R, Robinet A, Kouassi F X, Colin J

Abstract excerpt

We reported a case of a thrombosis of the retinal and central artery and vein in a 44-year-old patient, with high-grade T-cell lymphoma. Cardiovascular family history and a medical history of cerebral ischemia caused by in situ fibrinolysis, led to perform thorough hematologic and genetic examinations. These disclosed a prothrombin gene G 20210 a variant in a homozygous state. In a heterozygous state, this...

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PMID: 10609175

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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[Mixed retinal thrombosis in a patient carrying prothrombin gene mutation in a homozygote state].PMID 10609175Read ↗

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