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pro vyhledávání: '"Ambiguous external genitalia"'
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Publikováno v:
Volume: 9, Issue: 3 278-282
Konuralp Medical Journal
Konuralp Medical Journal
The SRD5A2 gene that encodes SRD5A2 enzyme is placed on chromosome 2p23. The coding region of the gene includes 5 exons that are translated into a 254-amino acid protein. To evaluate SRD5A2 gene that encodes SRD5A2 enzyme is placed on chromosome 2p23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5f3195f40a52ed6fc2ed8181e1610c
https://dergipark.org.tr/tr/pub/ktd/issue/32172/341688
https://dergipark.org.tr/tr/pub/ktd/issue/32172/341688
Publikováno v:
Reproduction in Domestic Animals. 49:E48-E52
Contents An eight-month-old female dog presented with ambiguous external genitalia. A thorough clinical examination together with various imaging techniques and a histology examination showed the presence of two testicles linked to both the Mullerian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50bb85cdec2d131621c4bec9c8656bdc
https://doi.org/10.1111/rda.12382
https://doi.org/10.1111/rda.12382
Autor:
S. Salamon, Rita Payan-Carreira, Izabela Szczerbal, Wojciech Niżański, Małgorzata Ochota, Stanisław Dzimira, Marek Świtoński, N. Mikolajewska, Joanna Nowacka-Woszuk
Publikováno v:
Chromosome Research. 22:393-437
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba0157dd3bf794013268c50189a5a205
https://doi.org/10.1007/s10577-014-9435-7
https://doi.org/10.1007/s10577-014-9435-7
Autor:
Stefanie Neuhauser, Mariana Peer, Achim D. Gruber, Heidi Kuiper, Christoph Lischer, Ottmar Distl, Johannes Handler, Christoph Klaus
Publikováno v:
Journal of Equine Veterinary Science. 32:117-122
Two phenotypically female Warmblood horses were presented at the Clinic for Horses owing to stallion-like behavior. One mare had an enlarged clitoris, whereas the other one showed no signs of ambiguous external genitalia. In both cases, intra-abdomin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cbdfd1c1c6e7ad4a87fbddb007cb550
https://doi.org/10.1016/j.jevs.2011.08.011
https://doi.org/10.1016/j.jevs.2011.08.011
Autor:
Ibrahim Aliyu
Publikováno v:
Medical Journal of Dr. D.Y. Patil University, Vol 8, Iss 6, Pp 766-768 (2015)
Ambiguous external genitalia could cause parental emotional trauma especially in an African setting where early gender assignment is an integral part of our culture. The most common cause of ambiguous external genital in Nigeria is 21-hydroxylase def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f64d935133bd64f6e91ea5d8d6db461b
http://www.mjdrdypu.org/article.asp?issn=0975-2870
http://www.mjdrdypu.org/article.asp?issn=0975-2870
Publikováno v:
Progresos de Obstetricia y Ginecología. 54:596-600
46 XY partial gonadal dysgenesis. Diagnosis in adulthood Abstract We report the case of a 24-year-old adult with ambiguous external genitalia, who had never been studied or treated, but who was labelled as a hermaphrodite in the country of origin. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b6600ba512350fa73ccb6db1b0f8f7e
https://doi.org/10.1016/j.pog.2011.06.006
https://doi.org/10.1016/j.pog.2011.06.006
Autor:
Chua Teck Seng, Wong Hock Boon
Publikováno v:
The Journal of The Asian federation of Obstetrics and Gynaecology. 1:14-22
Mixed gonadal dysgenesis is a condition characterised by presence of a testis on one side and a streak gonad on the other. Two such patients with the condition are described, one with a predominantly female external genitalia and the other with predo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11f0094f48bc927bcb21dfb31580d06f
https://doi.org/10.1111/j.1447-0756.1970.tb00128.x
https://doi.org/10.1111/j.1447-0756.1970.tb00128.x
Publikováno v:
Expert Review of Endocrinology & Metabolism. 4:53-65
17β-hydroxysteroid dehydrogenase deficiency is a rare autosomal recessive inherited disorder of sex development, affecting only 46,XY individuals. It is due to mutations in the HSD17B3 gene, encoding the 17β-hydroxysteroid-dehydrogenase type 3 enzy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e53c9de0ba2707f86a8ac7d97bffb389
https://doi.org/10.1586/17446651.4.1.53
https://doi.org/10.1586/17446651.4.1.53
Publikováno v:
Reproductive System & Sexual Disorders.
Pseudo-hermaphroditism is a rare condition which has much mystique to it. It is generally due to a deficiency of the enzyme 5α-reductase, responsible for the secretion and conversion of testosterone to dihydrotestosterone, which, in turn, defines th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14181b03c644a41fb3f1a593b1539609
https://doi.org/10.4172/2161-038x.1000162
https://doi.org/10.4172/2161-038x.1000162