"Turner 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 syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant.
| Descriptor ID |
D014424
|
| MeSH Number(s) |
C12.706.316.309.872 C12.706.316.795.750 C13.351.875.253.309.872 C13.351.875.253.795.750 C14.240.400.980 C14.280.400.980 C16.131.240.400.970 C16.131.260.830.835.750 C16.131.939.316.309.872 C16.131.939.316.795.750 C16.320.180.830.835.750 C19.391.119.309.872 C19.391.119.795.750
|
| Concept/Terms |
Turner Syndrome- Turner Syndrome
- Ullrich-Turner Syndrome
- Syndrome, Ullrich-Turner
- Ullrich Turner Syndrome
- Turner's Syndrome
- Turners Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Turner Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Turner Syndrome".
This graph shows the total number of publications written about "Turner Syndrome" by people in this website by year, and whether "Turner 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 |
|---|
| 1997 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2004 | 3 | 0 | 3 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2007 | 3 | 0 | 3 |
| 2008 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 4 | 1 | 5 |
| 2013 | 1 | 0 | 1 |
| 2014 | 1 | 1 | 2 |
| 2015 | 1 | 1 | 2 |
| 2016 | 4 | 1 | 5 |
| 2017 | 2 | 1 | 3 |
| 2018 | 3 | 0 | 3 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 5 | 0 | 5 |
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Below are the most recent publications written about "Turner Syndrome" by people in Profiles.
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The Effect of the Rate of Increase of Estrogen Replacement Therapy on Bone Mineral Density Accrual in Young Patients with Turner Syndrome. J Pediatr Adolesc Gynecol. 2023 Aug; 36(4):353-357.
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Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000-2017: A report from the National Birth Defects Prevention Network. Am J Med Genet A. 2023 05; 191(5):1339-1349.
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Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenat Diagn. 2023 02; 43(2):192-206.
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Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcome. Prenat Diagn. 2023 02; 43(2):183-191.
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Longitudinal investigation of cognition, social competence, and anxiety in children and adolescents with Turner syndrome. Horm Behav. 2023 03; 149:105300.
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Aortic tortuosity in Turner syndrome is associated with larger ascending aorta. Int J Cardiovasc Imaging. 2022 Nov; 38(11):2479-2490.
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Monosomy X in Female Mice Influences the Regional Formation and Augments the Severity of Angiotensin II-Induced Aortopathies. Arterioscler Thromb Vasc Biol. 2021 01; 41(1):269-283.
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Patient With Poor Prognosis, Family Wishes to Pursue All Options, Care Team Cannot Reach Consensus. Ann Thorac Surg. 2019 11; 108(5):1284-1286.
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Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years. Am J Med Genet A. 2019 10; 179(10):1987-2033.
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TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome. PLoS Genet. 2018 10; 14(10):e1007692.