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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.
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 6, 2020 · Triple X syndrome, also known as 47, XXX, Triple X, Triplo-X, or trisomy x is a sex chromosome aneuploidy, or chromosome abnormality, in which females have an additional X chromosome.
Aug 14, 2023 · Triple X syndrome is a genetic disorder caused by the presence of a third X chromosome. Although it’s genetic, it’s not usually passed down from a parent (inherited). Most cases are caused by errors that happen when chromosomes multiply and divide during the formation of egg or sperm cells.
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
Nov 25, 2021 · Triple X syndrome (also called trisomy X syndrome, XXX syndrome, or 47,XXX) is a rare genetic condition where females inherit an extra X chromosome. For some females with...
