Behçet disease (BD) is a chronic, relapsing, systemic vasculitis of unknown etiology with the
clinical features of oral and genital ulcers, cutaneous vasculitic lesions, ocular, articular …

Behçet Disease is a relapsing and remitting variable vessel vasculitis characterized by
recurrent mucocutaneous ulcers that can involve almost every organ system in the body …

Behçet's disease (BD) is a complex, recurring inflammatory disorder with autoinflammatory
and autoimmune components. This comprehensive review aims to explore BD's …

To ensure early identification of jBS, it is imperative to refine and develop diagnostic criteria
specifically tailored to pediatric populations. With a deeper understanding of the disease …

Behcet's disease (BD) is one of the most vision-threatening clinical entities of uveitis.
Although the etiopathogenesis of BD remains obscure, accumulating evidence has …

Objectives We aimed to assess first-degree relatives (FDRs) of Behçet's disease (BD)
patients for the presence of clinical symptoms and signs of BD and evaluate common …

Behçet's syndrome is a systemic inflammatory disorder of unknown origin, presenting with
diverse symptoms such as recurrent oral and genital ulcers, skin lesions, and uveitis, and …

Ocular inflammation represents one of the three cardinal manifestations of Behçet's disease
(BD) along with recurrent oral and genital ulceration. This study aims to characterize ocular …

La síndrome de Behçet (SB) és una malaltia sistèmica que es caracteritza per la presència
d'aftes orals i/o genitals de repetició, afectació cutània, articular, ocular, vascular …