Description. Trisomy X, also called triple X syndrome or 47,XXX, is characterized by the presence of an additional X chromosome in each of a female's cells. Although females with this condition may be taller than average, this chromosomal change typically causes no unusual physical features.
Feb 28, 2022
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Females with this genetic disorder have three X chromosomes instead of two. Symptoms can be mild or include developmental delays and learning disabilities.
Triple X syndrome, also called trisomy X or 47,XXX, is a genetic condition where a person is born with an extra X chromosome.
Most girls with triple X syndrome can grow up healthy, have normal sexual development and fertility, and lead productive lives.
Apr 4, 2024 · Disease Overview. 47, XXX (Trisomy X) is a disorder that affects females and is characterized by the presence of an additional X chromosome.
Triple X syndrome (Trisomy X) is a genetic condition that only affects females. Girls and women with triple X syndrome have an extra X chromosome. Most ...
Nov 25, 2021 · Triple X syndrome happens either when there is a problem with the sperm or egg during conception or because of an error in cell division during ...
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 ...
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.
Trisomy is a genetic condition that results in an extra copy of a chromosome. A person with trisomy will have 47 chromosomes instead of 46.