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  2. 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]

  3. 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 ...

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

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

    The hallmark of primary hypogonadism is low testosterone accompanied by increased FSH and LH. Secondary hypogonadism, on the other hand, occurs because of inadequate hypothalamic or pituitary ...

  5. 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 ...

  6. 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.

  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. Hypogonadotropic hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadotropic_hypogonadism

    Hypogonadotropic hypogonadism (HH), is due to problems with either the hypothalamus or pituitary gland affecting the hypothalamic-pituitary-gonadal axis (HPG axis). [1] Hypothalamic disorders result from a deficiency in the release of gonadotropic releasing hormone ( GnRH ), while pituitary gland disorders are due to a deficiency in the release ...

  9. Anovulation - Wikipedia

    en.wikipedia.org/wiki/Anovulation

    Treatment should be based on diagnosis of anovulation. Treatment varies based on the 4 most common causes of anovulation: polycystic ovarian syndrome (PCOS), hypogonadotropic hypogonadism (HA), primary ovarian insufficiency (POI), and hyperprolactinemia. [10]