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    XXYY Syndrome: Difference between revisions

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    Those with the the condition typically have [[Agenital|small testes]] that do not produce enough testosterone, which can lead to reduced facial and body hair, [[Secondary Sex Agenesis|poor muscle development]], breast growth, and infertility. Other common symptoms can include increased height, dental problems, problems with blood vessels in the legs, difficulty with language development, delayed development of motor skills, tremors that typically start in adolescence and increase with age, and an increased likelihood of several other physical and neurological conditions.<ref>https://rarediseases.info.nih.gov/diseases/5677/48xxyy-syndrome</ref> They typically also have [[AMAB Hypogonadism|AMAB hypogonadism]], and might also be classified under [[Aromatase Excess Syndrome|aromatase excess syndrome]].
    Those with the the condition typically have [[Agenital|small testes]] that do not produce enough testosterone, which can lead to reduced facial and body hair, [[Secondary Sex Agenesis|poor muscle development]], breast growth, and infertility. Other common symptoms can include increased height, dental problems, problems with blood vessels in the legs, difficulty with language development, delayed development of motor skills, tremors that typically start in adolescence and increase with age, and an increased likelihood of several other physical and neurological conditions.<ref>https://rarediseases.info.nih.gov/diseases/5677/48xxyy-syndrome</ref> They typically also have [[AMAB Hypogonadism|AMAB hypogonadism]], and might also be classified under [[Aromatase Excess Syndrome|aromatase excess syndrome]].

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


    == History ==
    == History ==
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