Autoimmune Lymphoproliferative Syndrome
"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
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MeSH Number(s) |
C15.604.515.138 C16.320.089 C20.111.288 C20.683.515.124
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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 |
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2010 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Autoimmune Lymphoproliferative Syndrome" by people in Profiles.
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ALPS or not? Blood. 2020 10 22; 136(17):1895-1896.
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Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease. J Clin Invest. 2020 01 02; 130(1):507-522.
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Diagnostic dilemma: ALPS versus Evans syndrome. Clin Immunol. 2017 10; 183:247-248.
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Why do T cells cause so much trouble? Blood. 2014 Mar 27; 123(13):1978.
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Development of disseminated histiocytic sarcoma in a patient with autoimmune lymphoproliferative syndrome and associated Rosai-Dorfman disease. Am J Surg Pathol. 2010 Apr; 34(4):589-94.