"Autoimmune Lymphoproliferative Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.
| Descriptor ID |
D056735
|
| MeSH Number(s) |
C15.604.515.138 C16.320.089 C20.111.288 C20.683.515.124
|
| Concept/Terms |
Autoimmune Lymphoproliferative Syndrome- Autoimmune Lymphoproliferative Syndrome
- Autoimmune Lymphoproliferative Syndromes
- Lymphoproliferative Syndrome, Autoimmune
- Lymphoproliferative Syndromes, Autoimmune
- Syndrome, Autoimmune Lymphoproliferative
- Syndromes, Autoimmune Lymphoproliferative
- Canale-Smith Syndrome
- Canale-Smith Syndromes
- Syndrome, Canale-Smith
- Syndromes, Canale-Smith
- Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
- Canale Smith Syndrome
- Syndrome, Canale Smith
Autoimmune Lymphoproliferative Syndrome Type 2B- Autoimmune Lymphoproliferative Syndrome Type 2B
- Caspase-8 Deficiency
- Caspase-8 Deficiencies
- Deficiencies, Caspase-8
- Deficiency, Caspase-8
- Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
- Autoimmune Lymphoproliferative Syndrome, Type IIb
- Caspase 8 Deficiency
- Caspase 8 Deficiencies
- Deficiencies, Caspase 8
- Deficiency, Caspase 8
|
Below are MeSH descriptors whose meaning is more general than "Autoimmune Lymphoproliferative Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Autoimmune Lymphoproliferative Syndrome".
This graph shows the total number of publications written about "Autoimmune Lymphoproliferative Syndrome" by people in this website by year, and whether "Autoimmune Lymphoproliferative Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Autoimmune Lymphoproliferative Syndrome" by people in Profiles.
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EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency. Front Immunol. 2018; 9:2400.
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STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds. Clin Immunol. 2017 08; 181:32-42.
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Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease. Haematologica. 2015 Sep; 100(9):1189-98.
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Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation. Clin Immunol. 2015 Jul; 159(1):84-92.
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A novel homozygous Fas ligand mutation leads to early protein truncation, abrogation of death receptor and reverse signaling and a severe form of the autoimmune lymphoproliferative syndrome. Clin Immunol. 2014 Dec; 155(2):231-7.
MeSH information
