"Schnitzler 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.
An extremely rare condition manifested as monoclonal IMMUNOGLOBULIN M dysproteinemia without features of lymphoproliferative disease, but with chronic urticaria, fever of unknown origin, disabling bone pain, hyperostosis, and increased erythrocyte sedimentation rate.
| Descriptor ID |
D019873
|
| MeSH Number(s) |
C20.683.780.640.700
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| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Schnitzler Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Schnitzler Syndrome".
This graph shows the total number of publications written about "Schnitzler Syndrome" by people in this website by year, and whether "Schnitzler Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Schnitzler Syndrome" by people in Profiles.
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Schnitzler syndrome in a patient with a family history of monoclonal gammopathy. Dermatol Online J. 2018 Jan 15; 24(1).