The xy female and swyer syndrome

We present the case of a patient with Swyer syndrome, and compare them with other cases of patients with a 46 XY karyotype, phenotypically female, such as in Congenital Adrenal Hyperplasia from deficiency of the 17 α hydroxylase/ 17 – 20 Lyase enzyme and in the Congenital Androgenic Insensitivity Syndrome.
Source: Urology Case Reports - Category: Urology & Nephrology Source Type: research