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14 de ago. de 2023 · Triple X syndrome is a rare genetic condition that affects only people assigned female at birth (AFAB). It’s also called trisomy X syndrome or 47,XXX. People are usually born with 46 chromosomes arranged in 23 pairs. (Chromosomes are the structures that carry your genetic information.) One copy of each chromosome in the pair comes from the ...
4 de abr. de 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. The characteristics (phenotype) associated with this chromosomal disorder varies widely, but most commonly includes language-based ...
Triple X syndrome is a genetic condition found in females only. About 1 in 1,000 girls have it. Girls with triple X syndrome — also known as XXX syndrome, trisomy X, and 47,XXX — might be taller than other girls. Other symptoms can include problems with spoken language and processing spoken words, coordination problems, and weaker muscles.
Síndrome triple X. El síndrome triple X, Trisomía XXX o 47,XXX es una aneuploidía cromosómica o cambio numérico de los cromosomas que se presenta en mujeres que poseen un cromosoma X extra. 1 Se trata de individuos femeninos con órganos sexuales atrofiados, fertilidad limitada y coeficiente intelectual normal.
6 de jul. de 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. The extra ...
47,XXX/46,XX - Generally speaking, the effects of triple X will be milder, lessened by the presence of cells with the normal number of X chromosomes in some tissues of the body 45,X/47,XXX - This is essentially a mosaic form of Turner syndrome (TS), although the presence of cells with an extra X chromosome will generally moderate the TS features,
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