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'''49,XXYYY syndrome''' is a [[intersex]] variation in which a [[CTM]] individual has two extra Y chromosomes and one extra X chromosome. It is a very rare variation amongst [[AMAB|DMAB]] individuals, and it has no estimated rarity. |
'''49,XXYYY syndrome''' is a [[intersex]] variation in which a [[CTM]] individual has two extra Y chromosomes and one extra X chromosome. It is a very rare variation amongst [[AMAB|DMAB]] individuals, and it has no estimated rarity. |
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Those with this variation tend to have facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age, and moderate intellectual disability |
Those with this variation tend to have facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age, and moderate intellectual disability<ref>[https://pubmed.ncbi.nlm.nih.gov/8330452/]</ref> This variation is often considered a subset or a related variation to [[Klinefelter Syndrome|kilnefelter syndrome]]. |
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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. |
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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