46, XX Disorders of Sex Development
"46, XX Disorders of Sex Development" 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.
Congenital conditions in individuals with a female karyotype, in which the development of the gonadal or anatomical sex is atypical.
| Descriptor ID |
D058489
|
| MeSH Number(s) |
C12.706.316.064 C13.351.875.253.064 C16.131.939.316.064 C19.391.119.064
|
| Concept/Terms |
Female Pseudohermaphroditism- Female Pseudohermaphroditism
- Female Pseudohermaphroditisms
- Pseudohermaphroditism, Female
- Pseudohermaphroditisms, Female
|
Below are MeSH descriptors whose meaning is more general than "46, XX Disorders of Sex Development".
Below are MeSH descriptors whose meaning is more specific than "46, XX Disorders of Sex Development".
This graph shows the total number of publications written about "46, XX Disorders of Sex Development" by people in this website by year, and whether "46, XX Disorders of Sex Development" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 2 | 0 | 2 |
| 2019 | 0 | 1 | 1 |
| 2021 | 3 | 0 | 3 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "46, XX Disorders of Sex Development" by people in Profiles.
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Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-K?ster-Hauser syndrome. HGG Adv. 2023 07 13; 4(3):100188.
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Functional characteristics of a broad spectrum of TBX6?variants in Mayer-Rokitansky-K?ster-Hauser syndrome. Genet Med. 2022 11; 24(11):2262-2273.
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Uterus transplantation worldwide: clinical activities and outcomes. Curr Opin Organ Transplant. 2021 12 01; 26(6):616-626.
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Implications of Ehlers-Danlos Syndrome in a Patient With Mayer-Rokitansky-K?ster-Hauser Syndrome. J Pediatr Adolesc Gynecol. 2021 Dec; 34(6):890-892.
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Perturbations of genes essential for M?llerian duct and W?lffian duct development in Mayer-Rokitansky-K?ster-Hauser syndrome. Am J Hum Genet. 2021 02 04; 108(2):337-345.
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Goldenhar syndrome associated with genital tract abnormality. BMJ Case Rep. 2019 Aug 28; 12(8).
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Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. Hum Mol Genet. 2018 04 01; 27(7):1228-1240.
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Assessing the Experience of Vaginal Dilator Use and Potential Barriers to Ongoing Use among a Focus Group of Women with Mayer-Rokitansky-K?ster-Hauser Syndrome. J Pediatr Adolesc Gynecol. 2017 Aug; 30(4):491-494.
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Deceased donor uterine transplantation. Fertil Steril. 2017 Mar; 107(3):e13.