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• W2090400518 endingPage "459" @default.
• W2090400518 startingPage "454" @default.
• W2090400518 abstract "Antiphospholipid syndrome (APS) is an autoimmune disease characterised by a heterogenous group of antibodies directed against negatively charged phospholipids including antiphospholipid antibodies (aPL), anticardiolipin antibodies (aCL) and β-2 glycoprotein I (aβ-2-GP1). The major features of this disorder include arterial and venous thrombosis and recurrent fetal loss. The vasculature of the eye is frequently involved and may be the presenting manifestation. A diagnosis of APS should be considered in a young patients without traditional thromboembolic risk factors presenting with ocular vaso-occlusive disease. Management of these patients involves a team-approach with a haematologist/oncologist or rheumatologist to manage the coagulation status of these patients to prevent further systemic vascular occlusions." @default.
• W2090400518 created "2016-06-24" @default.
• W2090400518 creator A5051656994 @default.
• W2090400518 creator A5060258624 @default.
• W2090400518 date "2010-08-07" @default.
• W2090400518 modified "2023-09-24" @default.
• W2090400518 title "Ocular manifestations of the antiphospholipid syndrome" @default.
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• W2090400518 doi "https://doi.org/10.1136/bjo.2010.182857" @default.
• W2090400518 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20693557" @default.
• W2090400518 hasPublicationYear "2010" @default.
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