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- W3023263746 abstract "The most common state of antiphospholipid syndrome (APS) is thrombophilic prone. However, the clinical manifestations of APS are not exclusive to vascular thrombosis or obstetric complications. Features associated with antiphospholipid antibody, not included in classification criteria, are also recognized: heart valve diseases, livedo reticularis, thrombocytopenia, nephropathy, and neurological disorders. Other nonthrombotic manifestations are also associated with antiphospholipid antibodies—the unique disease-causing pathogenic antibodies in a systemic autoimmune disorder. Clinical manifestations commonly found are deep vein thrombosis, thrombocytopenia, livedo reticularis, cerebrovascular accident, superficial thrombophlebitis, pulmonary embolism, and fetal loss. Hemolytic anemia, skin ulcers, epilepsy, myocardial infarction, amaurosis fugax, and digital necrosis are also found, although rarely." @default.
- W3023263746 created "2020-05-13" @default.
- W3023263746 creator A5035085923 @default.
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- W3023263746 date "2016-01-01" @default.
- W3023263746 modified "2023-09-26" @default.
- W3023263746 title "Clinical Manifestations" @default.
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- W3023263746 doi "https://doi.org/10.1016/b978-0-12-801917-7.00058-9" @default.
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