Unusual pattern of thrombotic events in young adult non-critically ill patients with COVID-19 may result from an undiagnosed inherited and acquired form of thrombophilia.
PMID: 34888860
2022
British journal of haematology
Abstract: The presence of JAK2-V617F, and FII-G20210A mutations was linked with SVT.
Abstract: We found a 55% prevalence of TGs mainly heterozygous coagulation factor II, thrombin (FII)-G20210A, Janus kinase 2 (JAK2)-V617F, protein-S, and antithrombin III deficiency with a high (76 9%) prevalence of venous UTEs, multiple vessels thrombosis, and recurrence rate among the TG versus non-TG subcohort.
SARS_CoV_2 mutation literature information.
PMID: 
2022
British journal of haematology
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