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- Dictionarytriple-X/ˌtrɪp(ə)lˈɛks/
adjective
- 1. relating to or denoting pornography of an explicit or extreme nature: informal "porn has moved out of the seedy bookshops and triple-X theatres"
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Apr 6, 2023 · Triple X syndrome (trisomy X or 47, XXX) is a genetic condition that occurs when a female is born with three X chromosomes in all or most of her cells rather than the usual two. Signs and symptoms of triple X syndrome vary widely.
Feb 2, 2022 · Triple X syndrome, also called trisomy X or 47,XXX, is a genetic disorder that affects about 1 in 1,000 females. Females normally have two X chromosomes in all cells — one X chromosome from each parent. In triple X syndrome, a female has three X chromosomes.
Trisomy X, also known as triple X syndrome and characterized by the karyotype [note 1] 47,XXX, is a chromosome disorder in which a female has an extra copy of the X chromosome. It is relatively common and occurs in 1 in 1,000 females, but is rarely diagnosed; fewer than 10% of those with the condition know they have it.
Triple X syndrome is a genetic condition where a person is born with an extra X chromosome. This condition only happens in people assigned female at birth (AFAB). Many people with triple X syndrome may have no symptoms and may not know they have the condition, or their symptoms could include being unusually tall and fertility issues.
May 30, 2023 · Triple X syndrome is a genetic disorder in which a female carries an extra X chromosome in each of her cells. It can be diagnosed prenatally or after birth. Menu
Trisomy X, which is also known as triple X syndrome or 47,XXX, is a chromosome disorder that occurs in females. Typically, individuals have 23 pairs, or 46 total chromosomes. The chromosome pairs are numbered 1-22, with the final pair being known as the sex chromosomes.
Oct 18, 2017 · Triple X, also called trisomy X and 47,XXX, is a genetic condition that occurs when a girl receives three X chromosomes from her parents. Typically, girls only receive two X chromosomes.
