 Turner Syndrome
"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
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| 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
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| Concept/Terms |
Turner Syndrome- Turner Syndrome
- Turner's Syndrome
- Turners Syndrome
- Ullrich-Turner Syndrome
- Syndrome, Ullrich-Turner
- Ullrich Turner Syndrome
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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 UAMS Profiles 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 |
|---|
| 2023 | 1 | 0 | 1 | | 2017 | 1 | 1 | 2 | | 2016 | 1 | 0 | 1 | | 2013 | 2 | 0 | 2 | | 2010 | 1 | 0 | 1 | | 2008 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 1997 | 1 | 0 | 1 | | 1996 | 1 | 0 | 1 | | 1995 | 1 | 0 | 1 |
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Below are the most recent publications written about "Turner Syndrome" by people in Profiles over the past ten years.
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Martin-Giacalone BA, Lin AE, Rasmussen SA, Kirby RS, Nestoridi E, Liberman RF, Agopian AJ, Carey JC, Cragan JD, Forestieri N, Leedom V, Boyce A, Nembhard WN, Piccardi M, Sandidge T, Shan X, Shumate CJ, Stallings EB, Stevenson R, Lupo PJ. 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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Philip J, Gupta D, Bleiweis MS, Pietra BA, Vyas HV. Hypoplastic left heart in Turner's syndrome: a primary indication for transplant? Cardiol Young. 2018 Mar; 28(3):458-460.
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Sharma R, Harris VM, Cavett J, Kurien BT, Liu K, Koelsch KA, Fayaaz A, Chaudhari KS, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Alarc?n-Riquelme M, Mariette X, Lessard CJ, Harley JB, Ng WF, Rasmussen A, Sivils KL, Scofield RH. Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sj?gren's Syndrome. Arthritis Rheumatol. 2017 11; 69(11):2187-2192.
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Lara DA, Ethen MK, Canfield MA, Nembhard WN, Morris SA. A population-based analysis of mortality in patients with Turner syndrome and hypoplastic left heart syndrome using the Texas Birth Defects Registry. Congenit Heart Dis. 2017 Jan; 12(1):105-112.
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