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  2. 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 .

  3. Sexual differentiation in humans - Wikipedia

    en.wikipedia.org/wiki/Sexual_differentiation_in...

    In the absence of a Y chromosome, the fetus will undergo female development. This is because of the presence of the sex-determining region of the Y chromosome, also known as the SRY gene. [5] Thus, male mammals typically have an X and a Y chromosome (XY), while female mammals typically have two X chromosomes (XX).

  4. 45,X/46,XY mosaicism - Wikipedia

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

    The 46,XY cells will continue to multiply at the same time as the 45,X cells multiply. The embryo, then the fetus, and then eventually the baby will have what is known as a 45,X/46,XY constitution. There are many chromosomal variations that cause the 45,X/46,XY karyotype, including malformation (isodicentricism) of the Y chromosomes, deletions ...

  5. 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.

  6. XY sex-determination system - Wikipedia

    en.wikipedia.org/wiki/XY_sex-determination_system

    In the XY sex-determination system, the female-provided ovum contributes an X chromosome and the male-provided sperm contributes either an X chromosome or a Y chromosome, resulting in female (XX) or male (XY) offspring, respectively. Hormone levels in the male parent affect the sex ratio of sperm in humans. [25]

  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. Sex differences in human physiology - Wikipedia

    en.wikipedia.org/wiki/Sex_differences_in_human...

    Externally, the most sexually dimorphic portions of the human body are the chest, the lower half of the face, and the area between the waist and the knees. [7] Males weigh more than females on average. [8] On average, males are taller than females by about 7% (12 cm). [9] [10]

  9. Development of the gonads - Wikipedia

    en.wikipedia.org/wiki/Development_of_the_gonads

    In the central mass a series of cords appear, and the periphery of the mass is converted into the tunica albuginea, thus excluding the surface epithelium from any part in the formation of the tissue of the testis. The cords of the central mass run together toward the future hilum and form a network which ultimately becomes the rete testis.