"Gonadal Dysgenesis" 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 number of syndromes with defective gonadal developments such as streak GONADS and dysgenetic testes or ovaries. The spectrum of gonadal and sexual abnormalities is reflected in their varied sex chromosome (SEX CHROMOSOMES) constitution as shown by the karyotypes of 45,X monosomy (TURNER SYNDROME); 46,XX (GONADAL DYSGENESIS, 46XX); 46,XY (GONADAL DYSGENESIS, 46,XY); and sex chromosome MOSAICISM; (GONADAL DYSGENESIS, MIXED). Their phenotypes range from female, through ambiguous, to male. This concept includes gonadal agenesis.
Descriptor ID |
D006059
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MeSH Number(s) |
C12.706.316.309 C13.351.875.253.309 C16.131.939.316.309 C19.391.119.309
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Gonadal Dysgenesis".
Below are MeSH descriptors whose meaning is more specific than "Gonadal Dysgenesis".
This graph shows the total number of publications written about "Gonadal Dysgenesis" by people in this website by year, and whether "Gonadal Dysgenesis" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1996 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Gonadal Dysgenesis" by people in Profiles.
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Noncytotoxic-Related Primary Ovarian Insufficiency in Adolescents: Multicenter Case Series and Review. J Pediatr Adolesc Gynecol. 2018 Dec; 31(6):597-604.
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Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region. J Med Genet. 2017 10; 54(10):705-709.
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Genetics of Reproductive Aging from Gonadal Dysgenesis through Menopause. Semin Reprod Med. 2017 03; 35(2):147-159.
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Dilated cardiomyopathy and ovarian dysgenesis in a patient with Malouf syndrome: a case report. Mol Med Rep. 2013 Nov; 8(5):1311-4.
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Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: clinical and functional characterization. Mol Hum Reprod. 2006 Jun; 12(6):401-6.
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Incomplete gonadal dysgenesis. Urol Int. 1996; 56(1):57-60.
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Gonadal dysgenesis and gonadoblastoma in situ in a female with Fraser (cryptophthalmos) syndrome. J Pediatr. 1986 Jun; 108(6):952-4.