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Blau syndrome is characterized by familial granulomatous arthritis, uveitis, and skin granulomas, comprising an autosomal dominantly inherited syndrome that overlaps both sarcoidosis and granuloma annulare. Restated, Blau syndrome is a rare autosomal dominant disorder characterized by granulomatous polyarthritis, panuveitis, cranial neuropathies, and exanthema. Camptodactyly is another feature, and Crohn's disease occurs in 30%. It is associated with mutations in the ''NOD2'' (a.k.a. CARD15) gene. == See also == * List of cutaneous conditions 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Blau syndrome」の詳細全文を読む スポンサード リンク
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