"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
|
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.
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Year | Major Topic | Minor Topic | Total |
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1998 | 1 | 0 | 1 |
2000 | 1 | 0 | 1 |
2002 | 0 | 1 | 1 |
2005 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2010 | 0 | 1 | 1 |
2011 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2018 | 2 | 0 | 2 |
2019 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Turner Syndrome" by people in Profiles.
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Aortic root dilation in a child with Marfan syndrome and mosaic Turner syndrome. Cardiol Young. 2020 Dec; 30(12):1976-1977.
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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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Early 2D/3D ultrasound diagnosis of pleural effusion in fetuses with Turner syndrome. J Clin Ultrasound. 2018 Nov; 46(9):585-587.
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Estrogen Replacement in Turner Syndrome: Literature Review and Practical Considerations. J Clin Endocrinol Metab. 2018 05 01; 103(5):1790-1803.
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Commentary: Launch of a quality improvement network for evidence-based management of uncommon pediatric endocrine disorders: Turner syndrome as a prototype. J Clin Endocrinol Metab. 2015 Apr; 100(4):1234-6.
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Maternal source of false-positive fetal sex chromosome aneuploidy in noninvasive prenatal testing. Obstet Gynecol. 2015 Feb; 125(2):390-392.
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Assessing the value of treatments to increase height. N Engl J Med. 2011 Mar 31; 364(13):1274-6.
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Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype. Eur J Med Genet. 2011 Mar-Apr; 54(2):161-4.
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Heart donors with underlying genetic syndromes. J Heart Lung Transplant. 2010 May; 29(5):588-9.
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Cruveilhier-Baumgarten disease in a patient with Turner syndrome: case report of a rare indication for liver transplantation. Liver Transpl. 2008 Mar; 14(3):299-302.