2,609
edits
m (Updating categories: removed Terminology) |
mNo edit summary |
||
(14 intermediate revisions by 6 users not shown) | |||
Line 1:
'''49,XXYYY syndrome''' is
Those with this variation tend to have facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age, and moderate [[Neurodivergent|intellectual disability
▲'''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.
▲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]].
== Studies ==
Medical professionals 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,
== Resources ==
[[Category:Intersex Traits]]
[[Category:Flagless Sexes]]
[[Category:Verified Resources]]
[[Category:Pages With No History Section]]
[[Category:Sex Category]]
|