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''Not to be confused with [[XXYY Syndrome]] or [[XXXYY Syndrome]].'' |
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'''49,XXYYY syndrome''' is a [[intersex]] condition in which a [[CTM]] has two extra Y chromosomes and one extra X chromosome. It is a very rare condition amongst [[AMAB|DMAB]] individuals, and it has no estimated rarity. |
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Those with this condition tend to have facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age, and moderate intellectual disability (such as autism.)<ref>[https://pubmed.ncbi.nlm.nih.gov/8330452/]</ref> This condition is often considered a subset or a related condition to [[Klinefelter Syndrome|kilnefelter syndrome]]. |
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⚫ | Medical proffesionals looked into tissues sampled for chromosome studies of external [[Ambiguous Genitalia|ambiguous genitalia]] and abdominal gonads, consisting of a left [[Ovotesticular|ovotestis]] and a right primitive testis, and found that they contained cells 46,XX, 47,[[XYY Syndrome|XXY]] and 49,XXYYY sex chromosomes.<ref>[https://www.karger.com/Article/PDF/129719][https://pubmed.ncbi.nlm.nih.gov/13959068/][https://op.europa.eu/en/publication-detail/-/publication/b7a528a6-2d20-4384-9e52-38579a0f3677]</ref> |
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== History == |
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This condition appears to have been discovered in 1967 or earlier, |
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== Resources == |
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https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1440-1754.1967.tb01693.x |
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[[Category:Intersex Traits]] |
[[Category:Intersex Traits]] |
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[[Category:Terminology]] |
[[Category:Terminology]] |