Update on ocular Behçet’s disease

Abstract

Behçet’s disease is among the chronic-relapsing, multisystemic inflammatory disorders that ARE characterized by obliterative vasculitis. Although it may affect almost all/any systems or organs, the key clinical manifestations are recurrent oral aphthous ulcers, genital ulcers, uveitis and skin lesions. Although most prevalent along the ancient Silk Route, extending from eastern Asia to the Mediterranean, Behçet’s disease is seen worldwide. This article aims to give a brief review on various aspects of Behçet’s disease, but particularly ocular involvement, with updated information.

Keywords::

• Behçet’s disease
• genital ulcers
• human leukocyte antigen B51
• recurrent oral aphthous ulcers
• treatment
• uveitis

Financial & competing interests disclosure

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.

No writing assistance was utilized in the production of this manuscript.