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'''49,XXXYY syndrome''' is
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.
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[[Category:Intersex Traits]]
[[Category:Flagless Sexes]]
[[Category:Pages With No History Section]]
[[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.