Article

Mutations of familial hemophagocytic lymphohistiocytosis (FHL) related genes and abnormalities of cytotoxicity function tests in patients with macrophage activation syndrome (MAS) occurring in systemic juvenile idiopathic arthritis (sJIA)

2014-01-01

Abstract

MAS is a severe complication of rheumatic diseases, mostly sJIA. Clinical and laboratory features are similar to those of FHL resulting from mutations in selected genes involved in the cytotoxicity pathway.

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Identifiers and source

Literature Corpus work: cbf49474-0f7c-5770-9891-29c69218035a
DOI: 10.1186/1546-0096-12-s1-p53
PMCID: PMC4184267

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