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

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...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Clin Transl Immunology
Asıl Yazarlar: Minson, Adrian, Voskoboinik, Ilia, Grigg, Andrew
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2021
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC8312240/
https://ncbi.nlm.nih.gov/pubmed/34336208
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cti2.1320
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