Hemophagocytic Lymphohistiocytosis Associated with Synergistic Defects of AP3B1 and ATM Genes: A Case Report and Literature Review

Hemophagocytic lymphohistiocytosis (HLH) is an overwhelming immune system activation that manifests as hyperinflammation and life-threatening multiple organ failure. However, the clinical manifestations of the systemic inflammatory response in sepsis and fulminant cytokine storm caused by HLH macrop...

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Detalles Bibliográficos
Autores principales: Yin, Guangjiao, Lu, Yasu, Pan, Huaqin, Deng, Bin, Wu, Sanyun, Peng, Zhiyong, Ye, Xujun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821123/
https://www.ncbi.nlm.nih.gov/pubmed/36614895
http://dx.doi.org/10.3390/jcm12010095

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821123/
https://www.ncbi.nlm.nih.gov/pubmed/36614895
http://dx.doi.org/10.3390/jcm12010095

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