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    XYYY Syndrome: Difference between revisions

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    (Created page with "'''48,XYYY syndrome''' is an intersex Y trisomy/chromosomal condition characterized by mild-moderate developmental delay, normal to mild intellectual disability, large, ir...")
     
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    '''48,XYYY syndrome''' is ana rare [[intersex]] Y trisomy/chromosomal condition characterized by mild-moderatehaving developmentalthree delay,Y normalchromones. toSymptoms mildcan intellectualinclude disability,delayed large,development irregularof teethlanguage withand/or poorlearning enameldisabilities. Physical features caused by this condition can include increased height, tallirregular statureteeth, 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 condition. [[Hypogonadism]] and infertility is frequently reported in adults. Children generally presenthave typical genitalia, whileso hypogonadismsome andmay infertilitynot isrealize frequentlythey reportedare affected until later in adultslife.<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>
     
    == Resources ==
    [[Category:Intersex Traits]]

    Revision as of 19:49, 12 November 2020

    48,XYYY syndrome is a rare intersex Y condition characterized by having three Y chromones. Symptoms can include delayed development of language and/or learning disabilities. Physical features caused by this condition 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 condition. 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][2]

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