XXYYY Syndrome: Difference between revisions

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 ''Not to be confused with [[XXYY Syndrome]], [[XXXYY Syndrome]], [[XXXYY Syndrome]].''
-'''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.
+'''49,XXYYY syndrome''' is a [[intersex]] variation in which a [[CTM]] 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.
-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]].
+Those with this variation 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 variation is often considered a subset or a related variation to [[Klinefelter Syndrome|kilnefelter syndrome]].
 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>
 == History ==
-This condition appears to have been discovered in 1967 or earlier,
+This variation appears to have been discovered in 1967 or earlier,
 == Resources ==