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{{Distinguish|XXYYY Syndrome|XXXY Syndrome|XXYY Syndrome|XXXXY Syndrome}} |
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[[File:XXXYY Syndrome.jpeg|thumb|The XXXYY Syndrome flag.]] |
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'''49,XXXYY syndrome''' is |
'''49,XXXYY syndrome''' is an [[intersex]] variation in which a [[CTM]] individual has two extra X chromosomes and one extra Y chromosome. It is a very rare variation amongst [[AMAB|DMAB]] individuals, and it has no estimated rarity.<ref>https://rarediseases.info.nih.gov/diseases/10922/49-xxxyy-syndrome</ref> |
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Symptoms of this include an abnormal face shape, a prominent forehead, widely spaced eyes, epicanthic folds, broad nasal bridge, prognathism, low-set rotated ears, a small jaw, club feet, abnormal feet prints, [[AMAB Hypogonadism|AMAB hypogonadism]], breast growth, delayed skeletal maturation, [[Agenital|microorchidism, a micropenis,]] and/or [[Ambiguous Genitalia|ambiguous genitalia.]] |
Symptoms of this include an abnormal face shape, a prominent forehead, widely spaced eyes, epicanthic folds, broad nasal bridge, prognathism, low-set rotated ears, a small jaw, club feet, abnormal feet prints, [[AMAB Hypogonadism|AMAB hypogonadism]], breast growth, delayed skeletal maturation, [[Agenital|microorchidism, a micropenis,]] and/or [[Ambiguous Genitalia|ambiguous genitalia.]] |
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Those with this variation tend to also have autism or be otherwise neurodivergent. This condition is considered similar to [[Klinefelter Syndrome|klinefelter syndrome]], and may or may not be considered a variation of it as well. |
Those with this variation tend to also have autism or be otherwise [[neurodivergent]]. This condition is considered similar to [[Klinefelter Syndrome|klinefelter syndrome]], and may or may not be considered a variation of it as well. |
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== Flag == |
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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. |
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The flag was created by Tumblr user dhddmods on July 31, 2024. The blue represents male-like anatomy. The grey represents hypoandrogenism. The yellow represents that this is an intersex variation. The pink represents female-like anatomy. Purple represents androgynous sex traits and potential ambiguous genitalia. The symbol is derived from the chromosomes of those with this variation.<ref>https://www.tumblr.com/dhddmods/757546864357834752/some-intersex-flags-part-3?source=share</ref> |
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==Resources== |
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<references /> |
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[[Category:Intersex Traits]] |
[[Category:Intersex Traits]] |
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[[Category:Pages With No History Section]] |
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* https://rarediseases.info.nih.gov/diseases/10922/49-xxxyy-syndrome |
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[[Category:Needs Resource Verification]] |
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Latest revision as of 18:48, 19 August 2024
49,XXXYY syndrome is an intersex variation in which a CTM individual has two extra X chromosomes and one extra Y chromosome. It is a very rare variation amongst DMAB individuals, and it has no estimated rarity.[1]
Symptoms of this include an abnormal face shape, a prominent forehead, widely spaced eyes, epicanthic folds, broad nasal bridge, prognathism, low-set rotated ears, a small jaw, club feet, abnormal feet prints, AMAB hypogonadism, breast growth, delayed skeletal maturation, microorchidism, a micropenis, and/or ambiguous genitalia.
Those with this variation tend to also have autism or be otherwise neurodivergent. This condition is considered similar to klinefelter syndrome, and may or may not be considered a variation of it as well.
Flag
The flag was created by Tumblr user dhddmods on July 31, 2024. The blue represents male-like anatomy. The grey represents hypoandrogenism. The yellow represents that this is an intersex variation. The pink represents female-like anatomy. Purple represents androgynous sex traits and potential ambiguous genitalia. The symbol is derived from the chromosomes of those with this variation.[2]