Hemophagocytic syndrome: Laboratory and molecular characterization
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening syndrome of fever, cytopenia, and organomegaly resulting from immune activation and cytokine storm. The syndrome can occur as a primary/familial form mostly affecting infants and young children or as an acquired form secondar...
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Main Authors: | Nooran Salem Yaseen, Sadiq Khalaf Ali, Hussam Saadi Aziz |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2024-12-01
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Series: | Iraqi Journal of Hematology |
Subjects: | |
Online Access: | https://journals.lww.com/10.4103/ijh.ijh_36_24 |
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