Pelvic Images of 46,XX Pure Gonadal Dysgenesis Patient after Hormone Replacement Therapy.
Taniguchi F.
J Minim Invasive Gynecol. 2023 Mar;30(3):167-168. doi: 10.1016/j.jmig.2022.12.003. Epub 2022 Dec 9.
Pure gonadal dysgenesis (46 XX type) with a familial pattern.
Kohmanaee S, Dalili S, Rad AH.
Adv Biomed Res. 2015 Aug 10;4:162. doi: 10.4103/2277-9175.162536. eCollection 2015.
Clinical features and management of 33 patients with 46,XX pure gonadal dysgenesis.
Huang H, Wang CQ, Tian QJ.
Gynecol Endocrinol. 2016 Dec;32(12):995-998. doi: 10.1080/09513590.2016.1190820. Epub 2016 Jun 2.
Twins discordant for 46,XX gonadal dysgenesis.
McDONOUGH PG, Tho PT, Byrd JR.
Fertil Steril. 1977 Mar;28(3):251-2. doi: 10.1016/s0015-0282(16)42434-9.
46 XX pure gonadal dysgenesis: an infrequent cause of primary amenorrhoea.
Pertusa S, Palacios A.
BMJ Case Rep. 2009;2009:bcr07.2008.0485. doi: 10.1136/bcr.07.2008.0485. Epub 2009 Apr 14.
46,XX gonadal absence: a variant of the XX pure gonadal dysgenesis?
Medina M, Kofman-Alfaro S, Pérez-Palacios G.
Acta Endocrinol (Copenh). 1982 Apr;99(4):585-7. doi: 10.1530/acta.0.0990585.
Familial dysgerminoma associated with 46, XX pure gonadal dysgenesis.
Namavar-Jahromi B, Mohit M, Kumar PV.
Saudi Med J. 2005 May;26(5):872-4.
[XX 'pure' gonadal dysgenesis and XYY syndrome].
Itoh N, Tsukamoto T.
Nihon Rinsho. 2004 Feb;62(2):305-8.
Familial ovarian dysgenesis in 46,XX females.
Vesely DL, Bower RH, Kohler PO, Char F.
Am J Med Sci. 1980 Nov-Dec;280(3):157-66. doi: 10.1097/00000441-198011000-00004.
Fertility issues in the management of patients with disorders of sex development.
Guercio G, Rey RA.
Endocr Dev. 2014;27:87-98. doi: 10.1159/000363633. Epub 2014 Sep 9.
