{"id":11268,"date":"2025-07-27T03:26:46","date_gmt":"2025-07-27T01:26:46","guid":{"rendered":"https:\/\/valintermed.com\/?p=11268"},"modified":"2025-07-27T03:26:46","modified_gmt":"2025-07-27T01:26:46","slug":"faktor-v-leydenskaya-trombofiliya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/factor-in-leidoscope-thromboembolism\/","title":{"rendered":"Factor V Leiden thrombophilia"},"content":{"rendered":"
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Factor V Leiden thrombophilia is an inherited disorder of hemostasis that results in an increased risk of blood clots. The condition is caused by a mutation in the factor V gene, which plays a key role in blood coagulation. Patients with the disorder may develop blood clots in the deep veins of the extremities (deep vein thrombosis) or the lungs (pulmonary embolism). It is these consequences that make Leiden thrombophilia an important topic for medical professionals. Given that the disorder can be asymptomatic, special attention is needed to diagnose and monitor it.<\/p>\n

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