Autoimmune lymphoproliferative syndrome (Q84637): Difference between revisions
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Síndrome linfoproliferativa autoimune (ALPS) é um transtorno genético associado a apoptose anormal de linfócitos, linfoproliferação e autoimunidade. Manifestações comuns são graves linfadenopatia e esplenomegalia, anemia hemolítica, neutropenia autoimune e púpura trombocitopênica imune. | |||
| description / en | description / en | ||
Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder associated with abnormal lymphocyte apoptosis, lymphoproliferation, and autoimmunity. Common features are severe lymphadenopathy and splenomegaly, haemolytic anaemia, autoimmune neutropaenia, and immune thrombocytopenia purpura. | |||
Revision as of 09:58, 15 August 2026
Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder associated with abnormal lymphocyte apoptosis, lymphoproliferation, and autoimmunity. Common features are severe lymphadenopathy and splenomegaly, haemolytic anaemia, autoimmune neutropaenia, and immune thrombocytopenia purpura.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1072688797 |
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| English | Autoimmune lymphoproliferative syndrome |
Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder associated with abnormal lymphocyte apoptosis, lymphoproliferation, and autoimmunity. Common features are severe lymphadenopathy and splenomegaly, haemolytic anaemia, autoimmune neutropaenia, and immune thrombocytopenia purpura. |
