Antiphospholipid syndrome (APS) is a prothrombotic condition with immune pathogenesis that is characterized by thrombosis in the venous or arterial vasculature and/or pregnancy morbidity, which occurs in the presence of persistent laboratory evidence of antiphospholipid antibodies (aPLs). aPLs are autoantibodies that target phospholipid-bound proteins, especially β2-glycoprotein I (β2-GPI). The presence of these antibodies is the defining feature of this syndrome; however, the mechanism by which aPLs cause a hypercoagulable state is not fully understood [1].
CITATION STYLE
Purohit, A., & Kumar, M. (2019). Antiphospholipid Syndrome. In Hematopathology: Advances in Understanding (pp. 349–359). Springer Singapore. https://doi.org/10.1007/978-981-13-7713-6_20
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