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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.
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.
Trisomy X, also known as triple X syndrome and characterized by the karyotype 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.
Jul 6, 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...
Apr 6, 2023 · Triple X syndrome (trisomy X) is a genetic condition that occurs when a female is born with three X chromosomes rather than two. Tall stature, low muscle tone, and developmental and social delays are common characteristics of the disorder.
Apr 4, 2024 · 47, XXX (Trisomy X) is a disorder that affects females and is characterized by the presence of an additional X chromosome. Normally, females have two X chromosomes, but females with 47, XXX have three X chromosomes.
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 triple X syndrome, the...
