 Syndrome
"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 symptom complex of unknown etiology, that is characteristic of a particular abnormality.
| Descriptor ID |
D013577
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| MeSH Number(s) |
C23.550.288.500
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| Concept/Terms |
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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 |
|---|
| 1980 | 0 | 3 | 3 | | 1981 | 0 | 3 | 3 | | 1982 | 0 | 4 | 4 | | 1983 | 0 | 3 | 3 | | 1984 | 0 | 2 | 2 | | 1985 | 0 | 5 | 5 | | 1986 | 0 | 8 | 8 | | 1987 | 0 | 5 | 5 | | 1988 | 0 | 7 | 7 | | 1989 | 0 | 11 | 11 | | 1990 | 0 | 6 | 6 | | 1991 | 0 | 10 | 10 | | 1992 | 0 | 6 | 6 | | 1993 | 0 | 11 | 11 | | 1994 | 0 | 6 | 6 | | 1995 | 0 | 5 | 5 | | 1996 | 0 | 10 | 10 | | 1997 | 0 | 11 | 11 | | 1998 | 0 | 9 | 9 | | 1999 | 0 | 10 | 10 | | 2000 | 0 | 8 | 8 | | 2001 | 0 | 5 | 5 | | 2002 | 0 | 16 | 16 | | 2003 | 0 | 18 | 18 | | 2004 | 0 | 18 | 18 | | 2005 | 0 | 15 | 15 | | 2006 | 0 | 13 | 13 | | 2007 | 0 | 20 | 20 | | 2008 | 0 | 15 | 15 | | 2009 | 0 | 14 | 14 | | 2010 | 1 | 13 | 14 | | 2011 | 0 | 7 | 7 | | 2012 | 0 | 5 | 5 | | 2013 | 0 | 13 | 13 | | 2014 | 0 | 6 | 6 | | 2015 | 0 | 6 | 6 | | 2016 | 0 | 7 | 7 | | 2017 | 0 | 6 | 6 | | 2018 | 0 | 10 | 10 | | 2019 | 0 | 4 | 4 | | 2020 | 0 | 6 | 6 | | 2021 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Syndrome" by people in Profiles.
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Prasanna P, Sriram CS, Rodriguez SH, Kohli U. Cardiovascular involvement in alpha-n-acetyl neuraminidase deficiency syndromes (sialidosis type I and II). Cardiol Young. 2021 May; 31(5):862-864.
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Schaenman JM, Diamond JM, Greenland JR, Gries C, Kennedy CC, Parulekar AD, Rozenberg D, Singer JP, Singer LG, Snyder LD, Bhorade S. Frailty and aging-associated syndromes in lung transplant candidates and recipients. Am J Transplant. 2021 06; 21(6):2018-2024.
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Gileta AF, Helgeson ML, Leonard JMM, Pyle LC, Subramanian HP, Arndt K, Hawkes CP, Del Gaudio D. Further delineation of a recognizable type of syndromic short stature caused by biallelic SEMA3A loss-of-function variants. Am J Med Genet A. 2021 03; 185(3):889-893.
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Blumkin L, Leibovitz Z, Krajden-Haratz K, Arad A, Yosovich K, Gindes L, Zerem A, Ben-Sira L, Lev D, Nissenkorn A, Kidron D, Dobyns WB, Malinger G, Bahi-Buisson N, Leventer RJ, Lerman-Sagie T. Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. Eur J Paediatr Neurol. 2020 May; 26:46-60.
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Nambot S, Faivre L, Mirzaa G, Thevenon J, Bruel AL, Mosca-Boidron AL, Masurel-Paulet A, Goldenberg A, Le Meur N, Charollais A, Mignot C, Petit F, Rossi M, Metreau J, Layet V, Amram D, Boute-Bénéjean O, Bhoj E, Cousin MA, Kruisselbrink TM, Lanpher BC, Klee EW, Fiala E, Grange DK, Meschino WS, Hiatt SM, Cooper GM, Olivié H, Smith WE, Dumas M, Lehman A. De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature. Eur J Hum Genet. 2020 06; 28(6):770-782.
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Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nat Med. 2020 01; 26(1):98-109.
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Mak CCY, Doherty D, Lin AE, Vegas N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung G, Barone Pritchard A, Yang S, Bend EG, Filippini F, Roadhouse C, Lebrun N, Mehaffey MG, Martin PM, Apple B, Millan F, Puk O, Hoffer MJV, Henderson LB, McGowan R, Wentzensen IM, Pei S, Zahir FR, Yu M, Gibson WT, Seman A, Steeves M, Murrell JR, Luettgen S, Francisco E, Strom TM, Amlie-Wolf L, Kaindl AM, Wilson WG, Halbach S, Basel-Salmon L, Lev-El N, Denecke J, Vissers LELM, Radtke K, Chelly J, Zackai E, Friedman JM, Bamshad MJ, Nickerson DA. MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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Burkardt DD, Tatton-Brown K, Dobyns W, Graham JM. Approach to overgrowth syndromes in the genome era. Am J Med Genet C Semin Med Genet. 2019 12; 181(4):483-490.
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Abdulkarim M, Karikari Y, Loomba RS, Anderson RH, Vricella L, El-Zein C. A Unique Case of Middle Aorta Syndrome With a "Corkscrew" Descending Aorta. World J Pediatr Congenit Heart Surg. 2019 11; 10(6):799-800.
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Dobyns WB, Mirzaa GM. Megalencephaly syndromes associated with mutations of core components of the PI3K-AKT-MTOR pathway: PIK3CA, PIK3R2, AKT3, and MTOR. Am J Med Genet C Semin Med Genet. 2019 12; 181(4):582-590.
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