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  2. Hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadism

    Hypogonadism resulting from defects of the gonads is referred to as hypergonadotropic hypogonadism or primary hypogonadism. Examples include Klinefelter syndrome and Turner syndrome. Mumps is known to cause testicular failure, and in recent years has been immunized against in the US. A varicocele can reduce hormonal production as well ...

  3. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    46,XX gonadal dysgenesis is characteristic of female hypogonadism with a karyotype of 46,XX. [8] Streak ovaries are present with non-functional tissues unable to produce the required sex steroid oestrogen. [9] Low levels of oestrogen effect the HPG axis with no feedback to the anterior pituitary to inhibit the secretion of FSH and LH. [9]

  4. Hypergonadotropic hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypergonadotropic_hypogonadism

    Hypergonadotropic hypogonadism (HH), also known as primary or peripheral/gonadal hypogonadism or primary gonadal failure, is a condition which is characterized by hypogonadism which is due to an impaired response of the gonads to the gonadotropins, follicle-stimulating hormone (FSH) and luteinizing hormone (LH), and in turn a lack of sex steroid production. [1]

  5. XY gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/XY_gonadal_dysgenesis

    XY complete gonadal dysgenesis, also known as Swyer syndrome, is a type of defect hypogonadism in a person whose karyotype is 46,XY. Though they typically have normal vulvas, [1] the person has underdeveloped gonads, fibrous tissue termed "streak gonads", and if left untreated, will not experience puberty.

  6. What Is Low Testosterone & What Causes It? - AOL

    www.aol.com/low-testosterone-causes-125700734.html

    Testosterone is the primary androgen — or male hormone — in your body. Low testosterone affects up to 39 percent of adult men in the US over the age of 45, and becomes increasingly prevalent ...

  7. XX gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/XX_gonadal_dysgenesis

    XX gonadal dysgenesis is a type of female hypogonadism in which the ovaries do not function to induce puberty in a person assigned female at birth, whose karyotype is 46,XX. [1] Individuals with XX gonadal dysgenesis have normal-appearing external genitalia as well as Müllerian structures (e.g., cervix, vagina, uterus).

  8. Kallmann syndrome - Wikipedia

    en.wikipedia.org/wiki/Kallmann_syndrome

    Primary amenorrhoea (failure to start menstruation). [8] Poorly defined secondary sexual characteristics. [3] Micropenis in 5-10% of male cases. [2] Cryptorchidism (undescended testicles) at birth. [2] Low levels of the gonadotropins LH and FSH. [3] Hypogonadism due to low levels of testosterone in men or oestrogen/progesterone in women. [3 ...

  9. Functional hypothalamic amenorrhea - Wikipedia

    en.wikipedia.org/wiki/Functional_hypothalamic...

    As women with FHA work to correct energy balance, especially female athletes and those recovering from eating disorder, recovery from hypogonadotropic hypogonadism may occur in a series of phases; there can be stages where the luteal phase is inadequate or may display lower sex steroid and gonadotropin levels for many years. [9]

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