References
- Lee PA, Houk CP, Ahmed SF, et al. Consensus statement on management of intersex disorders. International Consensus Conference on Intersex. Pediatrics 2006;118:e488–500.
- Hughes IA. Disorders of sex development: a new definition and classification. Best Pract Res Clin Endocrinol Metab 2008;22:119–34.
- Biason-Lauber A. WNT4, RSPO1, and FOXL2 in sex development. Semin Reprod Med 2012;30:387–95.
- Weinberg-Shukron A, Renbaum P, Kalifa R, et al. A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis. J Clin Invest 2015;125:4295–304.
- Kohmanaee S, Dalili S, Rad AH. Pure gonadal dysgenesis (46 XX type) with a familial pattern. Adv Biomed Res 2015;4:162.
- King TF, Conway GS. Swyer syndrome. Curr Opin Endocrinol Diabetes Obes 2014;21:504–10.
- Namavar-Jahromi B, Mohit M, Kumar PV. Familial dysgerminoma associated with 46, XX pure gonadal dysgenesis. Saudi Med J 2005;26:872–4.
- Pertusa S, Palacios A. 46 XX pure gonadal dysgenesis: an infrequent cause of primary amenorrhoea. BMJ Case Rep 2009. doi:10.1136/bcr.07.2008.0485.
- Michala L, Goswami D, Creighton SM, Conway GS. Swyer syndrome: presentation and outcomes. BJOG 2008;115:737–41.
- Grynberg M, Bidet M, Benard J, et al. Fertility preservation in Turner syndrome. Fertil Steril 2016;105:13–19.