The expanded second edition of this important work provides an up-to-date and comprehensive overview of Beh�et syndrome. New and updated chapters focus on recent advances in the areas of pathogenesis, the microbiome, genetics and epigenetics, clustering of symptoms, disease assessment and new treatment options.� The book examines how these developments have changed the way physicians� approach diagnosis, treatment, and management of Beh�et patients. It also analyzes the wide variety of clinical manifestations of the disease including mucocutaneous lesions, intraocular inflammation, central nervous system involvement,� deep vein thrombosis and other forms of major vascular disease. Building on the success of its predecessor, the�Second Edition�of�Beh�et Syndrome�is an invaluable resource for physicians, residents, fellows, and graduate students in rheumatology, dermatology, ophthalmology, neurology, gastroenterology, and internal medicine.