O16 A diagnosis of BehÇet’s Disease with secondary antiphospholipid syndrome
O16 A diagnosis of BehÇet’s Disease with secondary antiphospholipid syndrome
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Oxford: Oxford University Press
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English
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Oxford: Oxford University Press
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Abstract
Case report - Introduction
Behçet’s disease (BD) is a systemic inflammatory, variable-vessel vasculitis manifesting most commonly with recurrent oral or genital ulcers and uveitis. The heterogeneous presentation may also include skin, joint, gastrointestinal and central nervous system involvement. There is a geographical prevalence i...
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Full title
O16 A diagnosis of BehÇet’s Disease with secondary antiphospholipid syndrome
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8832427
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8832427
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ISSN
2514-1775
E-ISSN
2514-1775
DOI
10.1093/rap/rkab067.015
