Case Report: Generalised Panniculitis as a Post-COVID-19 Presentation in Aicardi-Goutières Syndrome Treated With Ruxolitinib

Aicardi-Goutières syndrome (AGS) is a rare hereditary early-onset encephalopathy. The syndrome was first described in 1984, and is characterised by upregulation of the type I interferon (IFN) pathway, which is involved in the host immune response against viral infections, including SARS-CoV-2. Whil...

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Main Authors: Abirami Pararajasingam (Author), Rachel E. Bradley (Author), Jennifer Evans (Author), Ashima Lowe (Author), Richard Goodwin (Author), Stephen Jolles (Author)
Format: Book
Published: Frontiers Media S.A., 2022-04-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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