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- W4386006143 abstract "Abstract Adamantiades–Behçet disease is a multisystem inflammatory disease of unknown aetiology, classified as a systemic vasculitis and as a neutrophilic dermatosis involving all types and sizes of blood vessels. It is characterized clinically by recurrent courses of oral aphthous ulcers, genital ulcers, skin lesions (papulopustules, erythema nodosum) and iridocyclitis/posterior uveitis. It is occasionally accompanied by arthritis and vascular, neurological, gastrointestinal or other manifestations. It is a rare disease with worldwide distribution but strongly varying prevalence; certain ethnic groups are mainly affected. It exhibits a genetically determined background with environmental triggering factor(s) probably involved. Diagnosis is defined by new clinical criteria. It presents a chronic, relapsing, progressive course and potentially poor prognosis (especially in males with systemic presenting signs)." @default.
- W4386006143 created "2023-08-20" @default.
- W4386006143 creator A5007042386 @default.
- W4386006143 date "2016-10-09" @default.
- W4386006143 modified "2023-10-12" @default.
- W4386006143 title "<scp>A</scp> damantiades– <scp>B</scp> ehçet Disease" @default.
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- W4386006143 doi "https://doi.org/10.1002/9781118441213.rtd0049" @default.
- W4386006143 hasPublicationYear "2016" @default.
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