Familial haemophagocytic lymphohistiocytosis (Q88710): Difference between revisions

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Latest revision as of 15:06, 15 August 2026

Familial hemophagocytic lymphohistiocytosis (FHL) is characterised by a macrophage activation syndrome presenting with unexplained high fever, irritability, general pain, oedema and hepatosplenomegaly, usually occurring after a healthy period that may range from several months after the birth to, more rarely, several years.

Language	Label	Description	Also known as
default for all languages	ID_950019605
English	Familial haemophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (FHL) is characterised by a macrophage activation syndrome presenting with unexplained high fever, irritability, general pain, oedema and hepatosplenomegaly, usually occurring after a healthy period that may range from several months after the birth to, more rarely, several years.