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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Detalles Bibliográficos
Autores principales: Minson, Adrian, Voskoboinik, Ilia, Grigg, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312240/
https://www.ncbi.nlm.nih.gov/pubmed/34336208
http://dx.doi.org/10.1002/cti2.1320

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312240/
https://www.ncbi.nlm.nih.gov/pubmed/34336208
http://dx.doi.org/10.1002/cti2.1320

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