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Autor:
Ameish Govindarajan MD, Frederick Venter MD, Akriti Chaudhry MD, Harsimranjit Kaur MD, Everardo Cobos MD, Greti Petersen MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 12 (2024)
Hemophagocytic lymphohistiocytosis (HLH) is a rare but often fatal condition characterized by a hyperinflammatory immune response leading to multiorgan failure. It is predominantly observed in the pediatric population and can be classified as familia
Externí odkaz:
https://doaj.org/article/ba66ee719cc043b88d18cbc0dc533755