"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
- Ullrich-Turner Syndrome
- Syndrome, Ullrich-Turner
- Ullrich Turner Syndrome
- Turner's Syndrome
- Turners 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 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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1995 | 1 | 0 | 1 |
1996 | 1 | 0 | 1 |
2006 | 1 | 0 | 1 |
2010 | 1 | 1 | 2 |
2019 | 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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Characteristics and progression of hearing loss in children with turner's syndrome. Laryngoscope. 2020 06; 130(6):1540-1546.
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Terminology for disorders of sex development: clarity or confusion? J Urol. 2011 Feb; 185(2):388-9.
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Laboratory guideline for Turner syndrome. Genet Med. 2010 Jan; 12(1):52-5.
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Selective alterations of white matter associated with visuospatial and sensorimotor dysfunction in turner syndrome. J Neurosci. 2006 Jun 28; 26(26):7007-13.
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Myelodysplasia associated with Turner syndrome. J Pediatr Hematol Oncol. 1996 Aug; 18(3):299-301.
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An atypical Turner syndrome patient with ring X chromosome mosaicism. Ann Clin Lab Sci. 1995 Jan-Feb; 25(1):60-5.
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Y chromosome--specific DNA sequences in Turner-syndrome mosaicism. Am J Hum Genet. 1987 Aug; 41(2):157-67.
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Upper moiety pelviureteric obstruction in infant with Turner syndrome. Urology. 1986 Feb; 27(2):158-9.
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Effects of long-term estrogen replacement therapy. I. Metabolic effects. Am J Obstet Gynecol. 1979 Mar 01; 133(5):525-36.