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'''49,XXXYY syndrome''' is a a [[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.
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
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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