 Gonadal Dysgenesis
"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 |
|---|
| 2000 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2019 | 0 | 1 | 1 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Gonadal Dysgenesis" by people in Profiles.
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Peard LM, Morin J, Flores V, Graham K, Taylor AS, Pope JC, Halstead V, Cost NG, Roberts EM, Makari JH, Cranford W, Saltzman AF. Gonadal tumors in a contemporary cohort of patients with differences in sex development undergoing surgery - A multi-site study from the Pediatric Urologic Oncology Working Group of the societies for pediatric urology. J Pediatr Urol. 2023 08; 19(4):399.e1-399.e8.
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Khanna AD, Duca LM, Kay JD, Shore J, Kelly SL, Crume T. Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System. Am J Cardiol. 2019 08 15; 124(4):618-626.
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Granados A, Alaniz VI, Mohnach L, Barseghyan H, Vilain E, Ostrer H, Quint EH, Chen M, Keegan CE. MAP3K1-related gonadal dysgenesis: Six new cases and review of the literature. Am J Med Genet C Semin Med Genet. 2017 06; 175(2):253-259.
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Alaniz VI, Kobernik EK, Dillman J, Quint EH. Utility of Ultrasound and Magnetic Resonance Imaging in Patients with Disorders of Sex Development Who Undergo Prophylactic Gonadectomy. J Pediatr Adolesc Gynecol. 2016 Dec; 29(6):577-581.
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Vrana PB, Fossella JA, Matteson P, del Rio T, O'Neill MJ, Tilghman SM. Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus. Nat Genet. 2000 May; 25(1):120-4.
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Wakimoto H, Takayasu S, Kurachi H, Komura H, Miyake A, Aono T, Tanizawa O, Matsumoto K. Clinical application of dihydrotestosterone (DHT) binding assay of cultured skin fibroblasts for the prospective differential diagnosis of testicular feminization syndrome (TFS). Asia Oceania J Obstet Gynaecol. 1985 Sep; 11(3):411-9.
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