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Dilemmas in the diagnosis and pathogenesis of atypical late‐onset familial haemophagocytic lymphohis...

Dilemmas in the diagnosis and pathogenesis of atypical late‐onset familial haemophagocytic lymphohis...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_284cd130720a4f88ac0b8f714b97c011

Dilemmas in the diagnosis and pathogenesis of atypical late‐onset familial haemophagocytic lymphohistiocytosis

About this item

Full title

Dilemmas in the diagnosis and pathogenesis of atypical late‐onset familial haemophagocytic lymphohistiocytosis

Publisher

Milton, Queensland: John Wiley & Sons, Inc

Journal title

Clinical & Translational Immunology, 2021, Vol.10 (7), p.n/a

Language

English

Formats

Publication information

Publisher

Milton, Queensland: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Objectives
A congenital loss of cytotoxic lymphocyte activity leads to a potentially fatal immune dysregulation, familial haemophagocytic lymphohistiocytosis. Until recently, this disease was uniformly associated with infants or very young children, but it appears now that the onset may be delayed for decades. As a result, some adults are being...

Alternative Titles

Full title

Dilemmas in the diagnosis and pathogenesis of atypical late‐onset familial haemophagocytic lymphohistiocytosis

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_284cd130720a4f88ac0b8f714b97c011

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_284cd130720a4f88ac0b8f714b97c011

Other Identifiers

ISSN

2050-0068

E-ISSN

2050-0068

DOI

10.1002/cti2.1320

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