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{{Distinguish|XXYYY Syndrome|XXXY Syndrome|XXYY Syndrome|XXXXY Syndrome}} |
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'''49,XXXYY syndrome''' is a rare gonosomal anomaly [[intersex]] bodily variation characterized by a eunuchoid habitus with gynecoid fat distribution and shape, normal to tall stature, intellectual disability of [https://tofansesmuna.tumblr.com/post/178483189587/start-using-support-levels-instead-of-functioning/amp medium to high support], distinctive facial features (e.g. prominent forehead, epicanthic folds, broad nasal bridge, prognathism), gynecomastia, [[hypogonadism]], [[Agenital#Cryptorchidism|cryptorchidism]], [[Agenital#Microorchidism|small penis]] and behavioral abnormalities (incl. solitary, passive disposition but prone to aggressive outbursts, autistic). Skeletal malformations, such as delayed bone age, fifth finger clinodactyly, elbow malformations and slow molar development, may also be associated.<ref>https://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=19887 |
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'''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.]] |
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https://rarediseases.info.nih.gov/diseases/10922/49-xxxyy-syndrome</ref> |
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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. |
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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:Flagless Sexes]] |
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[[Category:Pages With No History Section]] |
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[[Category:Verified Resources]] |
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Latest revision as of 23:49, 21 August 2022
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.