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Blau syndrome (BlauS) is a rare pediatric autoinflammatory disorder caused by NOD2 gene variants, characterized by granulomatous dermatitis, arthritis, and uveitis, with symptoms typically emerging by age 2. Early intervention with biologic therapies can prevent severe complications, but there is a lack of consensus on diagnostic criteria and treatment strategies due to the rarity of the condition. The review highlights the need for further research on epidemiology, pathophysiology, and management of BlauS

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putrijati29

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EN