BehÇet's disease is an inflammatory disorder of unknown cause, characterized by recurrent
oral aphthous ulcers, genital ulcers, uveitis, and skin lesions. 1, 2 All these common …

Behçet syndrome is a systemic vasculitis with an unknown aetiology affecting the small and
large vessels of the venous and arterial systems. The presence of symptom clusters …

The presence of symptom clusters, regional differences in disease expression and
similarities with, for example, Crohn's disease suggest multiple pathological pathways are …

Behçet's disease is a systemic vasculitis characterized by recurrent oral and genital ulcers,
and ocular inflammation, and which may involve the joints, skin, central nervous system and …

Behçet's disease usually begins with cutaneous manifestations, such as recurrent aphthous
stomatitis, genital ulcers, erythema nodosum-like lesions, papulopustular findings, and …

Behçet's disease is characterized by recurrent aphthous stomatitis, uveitis, genital ulcers,
and skin lesions. The role of the HLA-B* 51 gene has been confirmed in recent years …

The acne lesions characteristic of Behçet's syndrome are not sterile and are commonly
observed in combination with arthritis. The two main nodular skin lesions—superficial …

Behçet's disease is a multifaceted syndrome characterized by oral and genital ulcerations
and ocular abnormalities including keratitis, optic neuritis, and uveitis. The disease has …

This commentary provides an overview of recent advances concerning Behçet's disease
based on proceedings of the international conference on Behçet's disease sponsored by the …

Abstract The International Study Group's diagnostic criteria for Behçet's disease are gaining
acceptance and may be further refined before the decade is over. Previously neglected …