Swyer's Syndrome: In a Fifty-Year-Old Female

Affiliations

Cavit Culha et al. J Obstet Gynaecol India. 2012 Oct.

. 2012 Oct;62(5):571-4.

doi: 10.1007/s13224-011-0100-1. Epub 2012 Jan 17.

¹ Department of Endocrinology and Metabolism, Ankara Education and Research Hospital Ankara, Yavuzevler Sok. No: 30/16, Buyukesat, 06610 Ankara, Turkey.

No abstract available

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1. Conte AF, Grumbach MM. Disorders of sexual determination and differentiation. In: Gardner DG, Shobaek D, editors. Greenspan’s basic and clinical endocrinology. New York: McGraw-Hill, Appleton & Lange; 2007. pp. 562–610.
1. Battiloro E, Angeletti B, Tozzi MC, et al. A novel double nucleotide substitution in the HMG box of the SRY gene associated with Swyer Syndrome. Hum Genet. 1997;100:585–587. doi: 10.1007/s004390050557. - DOI - PubMed
1. Barbaro M, Oscarson M, Schoumans J, Staff J, Ivarsson SA, Wedell A, et al. Isolated 46, XY gonadal dysgenesis in two sisters caused by a Xp 21.2 interstitial duplication containing the DAX1 gene. J Clin Endocrinol Metab. 2007;92:3305–3313. doi: 10.1210/jc.2007-0505. - DOI - PubMed
1. Midro AT, Panasiuk B, Wolczynski S, et al. Clinical examinations, chromosomal and molecular DNA in patients with Swyer syndrome. Ginekol Pol. 1993;64:257–262. - PubMed
1. Scherer G, Held M, Erdel M, et al. Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations. Cytogenet Cell Genet. 1998;80:188–192. doi: 10.1159/000014978. - DOI - PubMed