Abstract
Adamantiades-Behçet’s Disease (ABD) is a vasculitis that affects multiple organ systems with relapsing chronic symptoms. Classic systemic findings include oral and genital ulcers as well as skin lesions. Ocular findings include anterior and posterior uveitis with vision-threatening complications such as macular edema and optic atrophy. The disease is strongly associated with Human Leukocyte Antigen (HLA)-B51 and predominantly found among people from the Mediterranean basin extending east. The etiology is unknown. Evidence indicates both genetic and environmental factors contribute to the pathogenesis. ABD is treated with steroids and immunomodulatory therapy including biologic agents.
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Lorch, A., Sobrin, L. (2017). Adamantiades-Behçet’s Disease. In: Papaliodis, G. (eds) Uveitis. Springer, Cham. https://doi.org/10.1007/978-3-319-09126-6_17
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DOI: https://doi.org/10.1007/978-3-319-09126-6_17
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