Familial haemophagocytic lymphohistiocytosis (Q88710): Difference between revisions
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13 August 2026
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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 |
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| 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. |
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CID11:ID_950019605
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dki-india-ID_950019605
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Concluído
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13 August 2026
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