Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetics of Primary Hemophagocytic Lymphohistiocytosis.

Advances in experimental medicine and biology - 1 Jan 2024

Karageorgos Spyridon, Platt Anna S, Bassiri Hamid

Abstract excerpt

Hemophagocytic lymphohistiocytosis (HLH) constitutes a rare, potentially life-threatening hyperinflammatory immune dysregulation syndrome that can present with a variety of clinical signs and symptoms, including fever, hepatosplenomegaly, and abnormal laboratory and immunological findings such as cytopenias, hyperferritinemia, hypofibrinogenemia, hypertriglyceridemia, elevated blood levels of soluble CD25...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cytotoxicity, Immunologic
Share to Genetic Predisposition to Disease
Share to Interleukin-2 Receptor alpha Subunit

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lymphohistiocytosis, Hemophagocytic

Share to Natural Killer T-Cells

Share to Recurrence

Share to Risk Factors

Source

Identifiers

PMID: 39117809
DOI: 10.1007/978-3-031-59815-9_7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetics of Primary Hemophagocytic Lymphohistiocytosis.PMID 39117809Read ↗

Genetics and pathophysiology of haemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Genetics of Familial Hemophagocytic Lymphohistiocytosis (HLH).Semantic proximity Read ↗

Pathogenesis of Hemophagocytic Lymphohistiocytosis.Semantic proximity Read ↗

Familial and acquired hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Hemophagocytic Lymphohistiocytosis in Adolescents and Young Adults: Genetic Predisposition and Secondary Disease.Semantic proximity Read ↗

Pathophysiology and epidemiology of hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Advances in the pathogenesis of primary and secondary haemophagocytic lymphohistiocytosis: differences and similarities.Semantic proximity Read ↗

Primary Hemophagocytic Lymphohistiocytosis: A Severe Immune Dysregulatory Disease with Various Genotypic Features and Outcomes: A Cross-Sectional Study from a Tertiary Pediatric CenterSemantic proximity Read ↗

Familial and Acquired Hemophagocytic LymphohistiocytosisSemantic proximity Read ↗

Primary and secondary hemophagocytic lymphohistiocytosis: clinical features, pathogenesis and therapy.Semantic proximity Read ↗

Familial Hemophagocytic Lymphohistiocytosis.Semantic proximity Read ↗

Hemophagocytic Lymphohistiocytosis: Lessons Learned from the Dark Side.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.