When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. 45,X/46,XY mosaicism - Wikipedia

    en.wikipedia.org/wiki/45,X/46,XY_mosaicism

    The clinical manifestations are highly variable, ranging from partial virilisation and ambiguous genitalia at birth, to patients with completely male or female gonads. Most individuals with this karyotype have apparently normal male genitalia , and a minority have female genitalia , with a significant number of individuals showing genital ...

  3. 46,XX/46,XY - Wikipedia

    en.wikipedia.org/wiki/46,XX/46,XY

    46,XX/46,XY chimeric or mosaic is associated with a wide spectrum of different physical presentations, with cases ranging from having a completely normal male or female phenotype [7] [8] [9] to some cases having ovotesticular syndrome. Due to this variation, genetic testing is the only way to reliably make a diagnosis.

  4. Disorders of sex development - Wikipedia

    en.wikipedia.org/wiki/Disorders_of_sex_development

    Complete androgen insensitivity syndrome causes a genetic male to have a vagina (often incompletely developed, nearly always blind-ending), breasts, and a clitoris; people with this form are raised as females. [25] Aphallia – a rare condition where a XY male is born without a penis. As of 2017, only 100 cases have been reported in literature ...

  5. Urethral syndrome - Wikipedia

    en.wikipedia.org/wiki/Urethral_syndrome

    [citation needed] The Skene's glands are embryologically related to the prostate gland in the male, thus urethral syndrome may share a comparable cause with chronic prostatitis. [ citation needed ] Possible non-infective causes include hormonal imbalance, [ 3 ] [ 4 ] trauma, allergies , anatomical features such as diverticula , and post ...

  6. Complete androgen insensitivity syndrome - Wikipedia

    en.wikipedia.org/wiki/Complete_androgen...

    Persons with a complete androgen insensitivity have a typical female external phenotype, despite having a 46,XY karyotype. [16] [17]Individuals with complete androgen insensitivity syndrome (grades 6 and 7 on the Quigley scale) are born with an external female phenotype, without any signs of genital masculinization, despite having a 46,XY karyotype. [18]

  7. 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.

  8. Battling fatigue: Why veterans are at risk for hormone imbalance

    www.aol.com/battling-fatigue-why-veterans-risk...

    Researchers don't fully understand how brain injuries impact hormones, but according to one study, as many as 80% of men with severe TBI experience low T following injury.

  9. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    Increased levels of these hormones will cause the body to not start puberty, not undergo menarche, and not develop secondary sex characteristics. [9] [10] If ovarian tissue is present and produces some amount of hormones, limited menstrual cycles can occur. [9] 46,XX gonadal dysgenesis can manifest from a variety of causes. [6]