XX male syndrome as a variant of congenital hypogonadotropic hypogonadism

• Sannikova Ekaterina S.
• Oleg Yu. Latyshev
• Lyubov’ N. Samsonova
• Elena V. Kiseleva
• Goar F. Okminyan
• Elvira P. Kasatkina

AbstractIt is a clinical case of one variant SRY-positive 46,XX testicular disorders of sex development with congenital hypergonadotropic hypogonadism with normal Leydig cells function. Today patient doesn't need testosterone replacement therapy.

Keywords:disorder of sex development, 46,XX Male syndrome, congenital hypergonadotropic hypogonadism

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