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Article

Advances in understanding the pathogenesis of HLH.

British journal of haematology - 1 Jun 2013

Usmani G Naheed, Woda Bruce A, Newburger Peter E

Abstract excerpt

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 uncontrolled...

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Identifiers

PMID: 23577835
DOI: 10.1111/bjh.12293

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23577835-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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