Biology of DSDs 6 Swyer Syndrome

>> YOUR LINK HERE: ___ http://youtube.com/watch?v=6doXQh962ls

Swyer syndrome, also known as Complete Gonadal Dysgenesis, is a sex development condition which affects individuals with a 46,XY karyotype. Because there is no testicular tissue to produce anti-Mullerian hormone and testosterone, individuals with Swyer develop female reproductive structures. • If you want to help improve medical research and psychological support for individuals with these conditions, you can donate to DSDFamilies (https://dsdfamilies.org/donate). • Biology of DSDs playlist: • • Disorders of Sex Development • Transcripts, sources, and membership at: • https://www.theparadoxinstitute.com/p... • References and additional reading: • [1] NIH. (2020). Swyer syndrome. Genetics Home Reference, National Library of Medicine. • [2] Jones, R., Lopez, K. (2014). Chapter 5: Sexual differentiation. Human Reproductive Biology, 4th edition. Elsevier. 95. • [3] LOCAH. (2018). The intersex masterpost. Medium. • [4] NIH. (2020). Swyer syndrome. Genetic and Rare Diseases Information Center. • [5] Azidah, AK. (2013). Swyer syndrome in a woman with 46,XY gonadal dysgenesis. Malaysian Family Physician, 8(2). • [6] Bagci, G., et al. (2011). Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters. Amer Soc Repro Med. • [7] Michala, L., et al. (2008). Swyer syndrome, presentation and outcomes. Journal of Obstetrics and Gynecology, 115(6). • [8] Nollman, J. (2013). An intersex story from X to Y. AIS DSD Support Group. • [9] Taneja, J., et al. (2016). Rare successful pregnancy in a patient with Swyer Syndrome.

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