"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.
A characteristic symptom complex.
| Descriptor ID |
D013577
|
| MeSH Number(s) |
C23.550.288.500
|
| Concept/Terms |
Syndrome- Syndrome
- Syndromes
- Symptom Cluster
- Cluster, Symptom
- Clusters, Symptom
- Symptom Clusters
|
Below are MeSH descriptors whose meaning is more general than "Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Syndrome".
This graph shows the total number of publications written about "Syndrome" by people in this website by year, and whether "Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 8 | 8 |
| 1995 | 0 | 13 | 13 |
| 1996 | 0 | 16 | 16 |
| 1997 | 0 | 18 | 18 |
| 1998 | 0 | 12 | 12 |
| 1999 | 0 | 21 | 21 |
| 2000 | 0 | 23 | 23 |
| 2001 | 0 | 21 | 21 |
| 2002 | 0 | 25 | 25 |
| 2003 | 0 | 29 | 29 |
| 2004 | 0 | 27 | 27 |
| 2005 | 0 | 34 | 34 |
| 2006 | 0 | 22 | 22 |
| 2007 | 1 | 43 | 44 |
| 2008 | 1 | 37 | 38 |
| 2009 | 1 | 38 | 39 |
| 2010 | 0 | 31 | 31 |
| 2011 | 0 | 16 | 16 |
| 2012 | 0 | 22 | 22 |
| 2013 | 0 | 20 | 20 |
| 2014 | 0 | 20 | 20 |
| 2015 | 0 | 18 | 18 |
| 2016 | 0 | 29 | 29 |
| 2017 | 0 | 17 | 17 |
| 2018 | 2 | 32 | 34 |
| 2019 | 0 | 22 | 22 |
| 2020 | 0 | 29 | 29 |
| 2021 | 0 | 22 | 22 |
| 2022 | 1 | 29 | 30 |
| 2023 | 0 | 19 | 19 |
| 2024 | 0 | 7 | 7 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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Clinical cases referring to the 2023 EACTS/STS Guidelines for diagnosing and treating acute and chronic syndromes of the aortic organ. Eur J Cardiothorac Surg. 2024 Sep 02; 66(3).
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Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genet Med. 2024 Nov; 26(11):101218.
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 Aug; 632(8026):832-840.
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Delphi Consensus on Diagnostic Criteria for LUMBAR Syndrome. J Pediatr. 2024 Sep; 272:114101.
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Medical algorithm: Diagnosis and management of adult food protein-induced enterocolitis syndrome. Allergy. 2024 Oct; 79(10):2881-2884.
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Egg-induced adult food protein-induced enterocolitis syndrome: Clinical phenotypes, natural history and immunological characteristics. J Allergy Clin Immunol Pract. 2024 Jun; 12(6):1657-1659.
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LUMBAR syndrome-OEIS complex overlap: A case series and review. Am J Med Genet A. 2024 07; 194(7):e63582.
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EACTS/STS Guidelines for Diagnosing and Treating Acute and Chronic Syndromes of the Aortic Organ. Ann Thorac Surg. 2024 Jul; 118(1):5-115.
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National multicentered retrospective review of clinical and intraoperative factors associated with the development of cerebellar mutism after pediatric posterior fossa tumor resection. Childs Nerv Syst. 2024 May; 40(5):1339-1347.
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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections. Genet Med. 2024 02; 26(2):101023.