Migraine, memory loss, and “multiple sclerosis ”. Neurological features of the antiphospholipid (Hughes’) syndrome

The antiphospholipid syndrome (APS, Hughes’ syndrome), first described in 1983, is a prothrombotic disease in which neurological events feature prominently. Strokes, transient ischaemic attacks, and headaches (including migraine) are important complications. However, it is clear that other neurologi...

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Bibliographic Details
Published in:Postgraduate medical journal Vol. 79; no. 928; pp. 81 - 83
Main Author: Hughes, G R V
Format: Journal Article Book Review
Language:English
Published: London The Fellowship of Postgraduate Medicine 01-02-2003
BMJ
Oxford University Press
BMJ Group
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Summary:The antiphospholipid syndrome (APS, Hughes’ syndrome), first described in 1983, is a prothrombotic disease in which neurological events feature prominently. Strokes, transient ischaemic attacks, and headaches (including migraine) are important complications. However, it is clear that other neurological symptoms, including diplopia, memory loss, ataxia, and “multiple sclerosis-like” features are common. A notable feature of Hughes’ syndrome is the clinical response to anticoagulants; features such as headache and memory loss often improving dramatically with appropriate warfarin dosage. APS may well become recognised as an important (and potentially treatable) cause of neurological disease.
Bibliography:local:0790081
ark:/67375/NVC-X7C4BM49-3
href:postgradmedj-79-81.pdf
Correspondence to:
 Dr Graham Hughes, Lupus Unit, St Thomas’ Hospital, London SE1 7EH; 
 graham.hughes@kcl.ac.uk
istex:7A4115F9591C7686ADF2C6FADC09E2C352EA7C3C
PMID:12612321
ObjectType-Case Study-3
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Review-1
ObjectType-Feature-5
ObjectType-Report-2
ObjectType-Article-4
ISSN:0032-5473
1469-0756
DOI:10.1136/pmj.79.928.81