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Heterozygous Mutation of Factor V Leiden Complicating Venous Thromboembolic Syndrome: A Case Report

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Heterozygous factor v leiden mutation increases thrombotic risk in young patients with unexplained vte,
In this case, a 32-year-old man with chronic smoking presented with unprovoked deep vein thrombosis and pulmonary embolism.
The analysis included a thorough thrombophilia work-up to guide personalized management in the case of combined genetic and acquired risks.
Early identification of thrombophilia disorders is crucial to prevent complications and recurrence in patients.

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Case report illustrates elevated thrombotic risk with factor v leiden and antiphospholipid syndrome in a young male.

Mehdi et al. (2025) studied this question.

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