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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. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    The syndrome is defined by the presence of at least one extra X chromosome in addition to a Y chromosome, yielding a total of 47 or more chromosomes rather than the usual 46. Klinefelter syndrome occurs randomly. The extra X chromosome comes from the father and mother nearly equally.

  4. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    The loss of the Y chromosome can occur from deletions, translocations, or migration diffenernce of paired chromosomes during cell division. [22] [23] The chromosomal loss results in partial expression of the SRY gene, giving rise to atypical development of the reproductive tract and altered hormone levels. [22] [23]

  5. 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]

  6. Disorders of sex development - Wikipedia

    en.wikipedia.org/wiki/Disorders_of_sex_development

    Turner syndrome (Ullrich-Turner syndrome and gonadal dysgenesis) – a condition that describes a female born with only one X chromosome or with an abnormal X chromosome, making her karotype 45,X0. It occurs in 1 in 2,000 to 5,000 females. [ 61 ]

  7. 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).

  8. Scientists solve the genetic puzzle of sex-related Y chromosome

    www.aol.com/news/scientists-solve-genetic-puzzle...

    Researchers on Wednesday unveiled the first complete sequence of the human Y chromosome, which is one of the two sex chromosomes - the X chromosome being the other - and is typically passed down ...

  9. XXYY syndrome - Wikipedia

    en.wikipedia.org/wiki/XXYY_syndrome

    48,XXYY syndrome is a condition related to the X and Y chromosomes (the sex chromosomes). People normally have 46 chromosomes in each cell. Two of the 46 chromosomes, known as X and Y, are called sex chromosomes because they help determine whether a person will develop male or female sex characteristics. Females typically have two X chromosomes ...