Ocular manifestations of the antiphospholipid syndrome

Published on Apr 1, 2011in British Journal of Ophthalmology3.611
· DOI :10.1136/BJO.2010.182857
Virginia Miraldi Utz9
Estimated H-index: 9
(Case Western Reserve University),
Johnny Tang15
Estimated H-index: 15
(Visual Sciences)
Sources
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.
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