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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. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    Gonadal dysgenesis; Specialty: Medical genetics Diagnostic method: pelvic examination (checking for maturation of external internal genitals), general examination (looking for secondary sexual characters), chromosome karyotyping, hormone levels like FSH, LH (which are increased in case of purely XX dysgenesis), family history: Treatment: surgery

  4. Hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadism

    Hypogonadism means diminished functional activity of the gonads—the testicles or the ovaries—that may result in diminished production of sex hormones.Low androgen (e.g., testosterone) levels are referred to as hypoandrogenism and low estrogen (e.g., estradiol) as hypoestrogenism.

  5. XX gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/XX_gonadal_dysgenesis

    Meanwhile, XY gonadal dysgenesis is known as PGD, 46,XY or Swyer syndrome. Patients with PGD have a normal chromosomal constellation but may have localized genetic alterations. XX gonadal dysgenesis is related to Swyer syndrome, since both conditions have the same phenotype and clinical issues; however in Swyer syndrome the karyotype is 46,XY ...

  6. Gonadal agenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_agenesis

    Gonadal agenesis is a rare condition where an individual lacks both gonads. If the karyotype is 46,XY and the individual otherwise has a male phenotype, it is called anorchia; this occurs in one of 20,000 male births. [1] The corresponding condition in an individual with a female phenotype and 46,XX phenotype is called bilateral ovarian ...

  7. Hypogonadotropic hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadotropic_hypogonadism

    Combined this causes the secretion of gonadal sex steroids and the initiation of folliculogenesis and spermatogenesis. The production of sex steroids forms a negative feedback loop acting on both the anterior pituitary and hypothalamus causing a pulsatile secretion of GnRH. [ 1 ]

  8. Late-onset hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Late-onset_hypogonadism

    As of 2016, the International Society for the Study of the Aging Male defines late-onset hypogonadism as a series of symptoms in older adults related to testosterone deficiency that combines features of both primary and secondary hypogonadism; the European Male Aging Study (a prospective study of ~3000 men) [10] defined the condition by the presence of at least three sexual symptoms (e.g ...

  9. Sexual anomalies - Wikipedia

    en.wikipedia.org/wiki/Sexual_anomalies

    Sexual anomalies, also known as sexual abnormalities, are a set of clinical conditions due to chromosomal, gonadal and/or genitalia variation.Individuals with congenital (inborn) discrepancy between sex chromosome, gonadal, and their internal and external genitalia are categorised as individuals with a disorder of sex development (DSD). [1]