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Mayer-Rokitansky-Küster-Hauser syndrome, known as MRKH, is a sex development condition in females which causes parts of the vagina, cervix, and uterus to be underdeveloped or absent. 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). Mayer-Rokitansky-Küster-Hauser syndrome. Genetics Home Reference, National Library of Medicine. [2] LOCAH. (2018). The Intersex Masterpost. Medium. [3] Witchel, S. (2018). Disorders of sex development. Best Practice and Research in Clinical Obstetrics and Gynecology, 48, 3. [4] CYWH. (2019). MRKH: General information for teens. Center for Young Women’s Health. [5] Amies, AM., et al. (2018). Mullerian agenesis--diagnosis, management, and treatment. American College of Obstet & Gynec, 728. [6] Ernst, M. (2016). The lived experience of MRKH, sharing health information with peers. Pediatric and Adolescent Gynecology, 29(2). [7] Fontana, L., et al. (2017). Genetics of Mayer-Rokitansky-Kuster-Hauser syndrome. Clinical Genetics, 91, 233-246. [8] Londra, L., et al. (2015). Mayer-Rokitansky-Kuster-Hauser syndrome, a review. International Journal of Women's Health, 7, 865-870. [9] Pizzo, A., et al. (2013). Mayer-Rokitansky-Kuster-Hauser Syndrome. Embryology, Genetics and Clinical and Surgical Treatment. ISRN Obstetrics and Gynecology. MRKH support groups and foundations: [1] Beautiful You MRKH (https://www.beautifulyoumrkh.org) [2] MRKH Connect (https://mrkhconnect.co.uk) [3] Young Women's Health MRKH resources (https://youngwomenshealth.org/mrkh-al...)