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Advances in understanding the pathogenesis of HLH

✍ Scribed by Usmani, G. Naheed; Woda, Bruce A.; Newburger, Peter E.

Book ID: 120271815
Publisher: John Wiley and Sons
Year: 2013
Tongue: English
Weight: 367 KB
Volume: 161
Category: Article
ISSN: 0007-1048
DOI: 10.1111/bjh.12293

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## Summary Haemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory disorder resulting from immune dysfunction reflecting either primary immune deficiency or acquired failure of normal immune homeostasis. Familial HLH includes autosomal recessive and X‐linked disorders characterized by unco

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