Behçet's disease (BD) is a chronic relapsing and remitting vasculitis of unknown aetiology. It
has the capacity to affect almost all organ systems because of its potential to involve both …

Autoimmune and dysimmune inflammatory mechanisms on a genetically susceptible
background are implicated in the etiology of Behçet's Disease (BD). Heat-shock protein-65 …

Vascular inflammation in small to large veins and arteries contributes substantially to
mortality above that of the general population in Behçet's disease. Recent data verified also …

Objective. To assess adherence to published guidelines for the treatment of Behçet's
syndrome (BS) in two geographic areas. Methods. We extracted guideline statements from …

Behcet's disease (BD) is a rare condition in sub-Saharan Africa. It often manifests as
recurrent oral and genital aphthous ulcers with ocular features and infrequently involving …

Behçet's disease (BD) is a systemic inflammatory disorder whose clinical hallmark is
recurrent oral and genital ulcers variably associated with skin and organ involvement. BD is …

Behcet's disease is a rare autoimmune systemic vasculitis. It usually presents with a
symptom complex involving primarily mucocutaneous lesions, genital lesions, and uveitis …

Diagnosis can be difficult when the classic symptoms of an uncommon illness emerge
weeks after presentation. A 51-year-old African American man presented to the emergency …