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This is an accepted version of this page This is the latest accepted revision, reviewed on 24 February 2025. Atypical congenital variations of sex characteristics This article is about intersex in humans. For intersex in other animals, see Intersex (biology). Not to be confused with Hermaphrodite. Intersex topics Human rights and legal issues Compulsory sterilization Discrimination Human ...
Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly where a male has an extra X chromosome. [10] These complications commonly include infertility and small, poorly functioning testicles (if present).
XXY is a 2007 Argentine drama film written and directed by Lucía Puenzo and starring Ricardo Darín, Valeria Bertuccelli, Inés Efron and Martín Piroyansky.Based on the short story Cinismo (Cynicism), included in the book Chicos (Boys) by author Sergio Bizzio, the film tells the story of a 15-year-old intersex person, the way her family copes with her condition and the ultimate decision that ...
Women first competed at the Olympic Games in 1900, with an increased programme available for women to enter from 1924. [9] Prior to 1936, sex verification may have been done ad hoc, but there were no formal regulations; [2] the existence of intersex people was known about, though, and the Olympics began "dealing with" – acknowledged and sought to regulate [1] – intersex athletes ahead of ...
Klinefelter syndrome (47,XXY and XXY syndrome) – a condition that describes a male born with at least one extra X chromosome. Though the most common variation is 47,XXY, a man may also be 48,XXXY or 49,XXXXY. It is a common occurrence, affecting 1 in 500 to 1,000 men. [44]
The new binary definitions exclude references to gender, erase the identities of gender-diverse and intersex individuals, and may lead to physical and mental health harm. Robert F. Kennedy Jr ...
Saying otherwise jeopardizes not only intersex and transgender people, ... (in which people have XXY chromosomes) and higher risk of diabetes, autoimmune disorders, cardiovascular issues and poor ...
The cause of the condition lies in conception or utero with the aggregation of two distinct zygotes or blastocysts (one of which expresses 46,XX and the other of which expresses 46,XY) into a single embryo, [4] which subsequently leads to the development of a single individual with two distinct cell lines, instead of a pair of fraternal twins.