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Diagnosis of antiphospholipid syndrome (APS) requires persistent presence of lupus anticoagulant (LAC), anticardiolipin (aCL) IgG/IgM, or anti‐β2 glycoprotein I (aβ2GPI) IgG/IgM antibodies. Other antiphospholipid antibodies (aPL) such as antiphosphatidylserine/prothrombin antibodies… Click to show full abstract
Diagnosis of antiphospholipid syndrome (APS) requires persistent presence of lupus anticoagulant (LAC), anticardiolipin (aCL) IgG/IgM, or anti‐β2 glycoprotein I (aβ2GPI) IgG/IgM antibodies. Other antiphospholipid antibodies (aPL) such as antiphosphatidylserine/prothrombin antibodies (aPS/PT) are promising in assessment of thrombotic APS (TAPS).
Keywords:
antiphosphatidylserine prothrombin;
antiphospholipid syndrome;
prothrombin antibodies;
lupus anticoagulant;
antiphospholipid antibodies
Journal Title: Journal of Thrombosis and Haemostasis
Year Published: 2022
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Journal Title: Journal of Thrombosis and Haemostasis
Year Published: 2022
Link to full text (if available)
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recommendations!