A Rare STXBP2 Mutation in Severe COVID-19 and Secondary Cytokine Storm Syndrome

Background: Primary (familial) hemophagocytic lymphohistiocytosis (pHLH) is a potentially lethal syndrome of infancy, caused by genetic defects in natural killer (NK) cell and CD8 T cell cytotoxicity, leading to hyperinflammation, elevated cytokine levels, and a disorganized immune response resultin...

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Detalles Bibliográficos
Autores principales: Reiff, Daniel D., Zhang, Mingce, Smitherman, Emily A., Mannion, Melissa L., Stoll, Matthew L., Weiser, Peter, Cron, Randy Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877603/
https://www.ncbi.nlm.nih.gov/pubmed/35207437
http://dx.doi.org/10.3390/life12020149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8877603/
https://www.ncbi.nlm.nih.gov/pubmed/35207437
http://dx.doi.org/10.3390/life12020149

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