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 lymphohistiocytosis
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Milton, Queensland: John Wiley & Sons, Inc
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Language
English
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Publisher
Milton, Queensland: John Wiley & Sons, Inc
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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...
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Dilemmas in the diagnosis and pathogenesis of atypical late‐onset familial haemophagocytic lymphohistiocytosis
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TN_cdi_doaj_primary_oai_doaj_org_article_284cd130720a4f88ac0b8f714b97c011
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_284cd130720a4f88ac0b8f714b97c011
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ISSN
2050-0068
E-ISSN
2050-0068
DOI
10.1002/cti2.1320