Successful treatment of Sneddon Syndrome with high dose intravenous immunoglobulin

Abstract Sneddon Syndrome is an orphan disease characterized by the clinical presence of livedo racemosa and cerebrovascular ischaemia. Its pathophysiology remains inadequately understood and no validated treatment modality has been established. In this case report of a 37‐year‐old woman, we present...

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主要な著者: Markus Reitmajer (著者), Stephan Forchhammer (著者), Toni Silber (著者)
フォーマット: 図書
出版事項: Wiley, 2024-12-01T00:00:00Z.
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3rd Floor Main Library

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