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. Whils...

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Detalles Bibliográficos
Autores principales: Pararajasingam, Abirami, Bradley, Rachel E., Evans, Jennifer, Lowe, Ashima, Goodwin, Richard, Jolles, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085217/
https://www.ncbi.nlm.nih.gov/pubmed/35547545
http://dx.doi.org/10.3389/fped.2022.837568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085217/
https://www.ncbi.nlm.nih.gov/pubmed/35547545
http://dx.doi.org/10.3389/fped.2022.837568

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