Presumed Antiphospholipid Syndrome And Thrombotic Thrombocytopenic Purpura: An Infrequent Association
CLINICAL CASE REPORTS(2019)
Abstract
Antiphospholipid syndrome (APS) is an autoimmune disease that demonstrates antiphospholipid antibodies that cause hypercoagulability and leads to venous and arterial thrombosis. Autoantibodies to a disintegrin-like and metalloprotease with thrombospondin type I motif, member 13 (ADAMTS 13) play a role in the microthrombosis of thrombotic thrombocytopenic purpura in APS patients.
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Key words
ADAMTS13, antiphospholipid syndrome, disintegrin-like and metalloprotease, thrombotic thrombocytopenic purpura
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