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  2. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    Mixed gonadal dysgenesis, also known as X0/XY mosaicism or partial gonadal dysgenesis, [21] is a sex development difference associated with sex chromosome aneuploidy and mosaicism of the Y chromosome. [14] Mixed gonadal dysgenesis is the presence of two or more germ line cells. [23]

  3. 45,X/46,XY mosaicism - Wikipedia

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

    45,X/46,XY mosaicism, also known as X0/XY mosaicism and mixed gonadal dysgenesis, [1] is a mutation of sex development in humans associated with sex chromosome aneuploidy and mosaicism of the Y chromosome. It is a fairly rare chromosomal disorder at birth, with an estimated incidence rate of about 1 in 15,000 live births. [2]

  4. 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 .

  5. Disorders of sex development - Wikipedia

    en.wikipedia.org/wiki/Disorders_of_sex_development

    Mixed gonadal dysgenesis – a condition of unusual and asymmetrical gonadal development leading to an unassigned sex differentiation. A number of differences have been reported in the karyotype, most commonly a mosaicism 45,X/ 46,XY. [52]

  6. Sex chromosome anomalies - Wikipedia

    en.wikipedia.org/wiki/Sex_chromosome_anomalies

    46, XX gonadal dysgenesis; 46, XY gonadal dysgenesis, also known as Swyer syndrome; 46, XX male syndrome, also known as de la Chapelle syndrome; In this list, the karyotype is summarized by the number of chromosomes, followed by the sex chromosomes present in each cell.

  7. Androgen insensitivity syndrome - Wikipedia

    en.wikipedia.org/wiki/Androgen_insensitivity...

    Mixed gonadal dysgenesis (45,XO/46,XY karyotype) Tetragametic chimerism (46,XX/46,XY karyotype) Androgen biosynthetic dysfunction in 46,XY individuals: Luteinizing hormone (LH) receptor mutations; Smith–Lemli–Opitz syndrome (associated with intellectual disability) Lipoid congenital adrenal hyperplasia; 3β-hydroxysteroid dehydrogenase 2 ...

  8. Microplastics Are in All of Us. Just How Bad Is That, Really?

    www.aol.com/microplastics-us-just-bad-really...

    Tiny plastic particles have been found throughout the human body, but researchers say they’re just starting to understand the impact. When Jaime Ross, PhD, a neuroscientist and assistant ...

  9. Sex assignment - Wikipedia

    en.wikipedia.org/wiki/Sex_assignment

    In the 1950s, endocrinologists developed a basic understanding of the major intersex conditions such as congenital adrenal hyperplasia (CAH), androgen insensitivity syndrome, and mixed gonadal dysgenesis. The discovery of cortisone allowed survival of infants with severe CAH for the first time. New hormone tests and karyotypes allowed more ...