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    XYYY Syndrome: Difference between revisions

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    [[File:Xyyy syndrome.png|thumb|XYYY syndrome flag.]]
    [[File:Xyyy syndrome.png|thumb|XYYY syndrome flag.]]
    ''Not to be confused with [[XYYYY Syndrome|XYYYY Syndrome.]]''
    :''{{Distinguish|XYYYY Syndrome|XYY Syndrome|XXYYY Syndrome}}''

    '''48,XYYY syndrome''' is a rare [[intersex]] variation found within [[AMAB]]/[[CTM]] individuals. This variation is characterized by having three Y chromosomes instead of having the usual amount (XY.)
    '''48,XYYY syndrome''' is a rare [[intersex]] variation found within [[AMAB]]/[[CTM]] individuals. This variation is characterized by having three Y chromosomes instead of having the usual amount (XY.)


    Symptoms can include delayed development of language and/or learning disabilities. Physical features caused by this variation can include increased height, irregular teeth, and acne. Radioulnar stenosis (an abnormal connection between the bones of the forearm) and clinodactyly (a bent finger or toe) have also been associated with the variation. [[Hypogonadism]] and infertility is frequently reported in adults. Children generally have typical genitalia so some may not realize they are affected until later in life.<ref>https://beyond-mogai-pride-flags.tumblr.com/post/184220322075/xyyy-pride-flag</ref><ref>https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99329</ref>
    Traits of this variation may include delayed development of language and/or learning disabilities. Physical features caused by this variation can include increased height, irregular teeth, and acne. Radioulnar stenosis (an abnormal connection between the bones of the forearm) and clinodactyly (a bent finger or toe) have also been associated with the variation. [[Hypogonadism]] and infertility is frequently reported in adults. Children generally have typical genitalia so some may not realize they are affected until later in life.<ref>https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=99329</ref>

    It is important to note that not all the symptoms listed in this page are guaranteed to occur in someone with this variation, as someone may only experience one or several of these symptoms, yet still hold the variation.


    == Flag ==
    == Flag ==
    The flag was coined by beyond-mogai-pride-flags on April 16th of 2019. The colors have no confirmed meaning, however the the X and three Ys clearly represents the variation within itself.
    The flag was coined by beyond-mogai-pride-flags on April 16th of 2019. The colors have no confirmed meaning, however the the X and three Ys clearly represents the variation within itself.<ref>https://beyond-mogai-pride-flags.tumblr.com/post/184220322075/xyyy-pride-flag</ref>


    == Resources ==
    == Resources ==
    [[Category:Intersex Traits]]
    [[Category:Intersex Traits]]
    [[Category:Terminology]]
    [[Category:Verified Resources]]
    [[Category:Sex Category]]

    Latest revision as of 18:43, 21 January 2023

    XYYY syndrome flag.

    48,XYYY syndrome is a rare intersex variation found within AMAB/CTM individuals. This variation is characterized by having three Y chromosomes instead of having the usual amount (XY.)

    Traits of this variation may include delayed development of language and/or learning disabilities. Physical features caused by this variation can include increased height, irregular teeth, and acne. Radioulnar stenosis (an abnormal connection between the bones of the forearm) and clinodactyly (a bent finger or toe) have also been associated with the variation. Hypogonadism and infertility is frequently reported in adults. Children generally have typical genitalia so some may not realize they are affected until later in life.[1]

    Flag

    The flag was coined by beyond-mogai-pride-flags on April 16th of 2019. The colors have no confirmed meaning, however the the X and three Ys clearly represents the variation within itself.[2]

    Resources

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