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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 ...
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. Most females with trisomy X have normal sexual development and are ...
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 ...
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 ...
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6 de abr. de 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. Some people may have no signs or symptoms, while others may experience developmental, psychological, and medical symptoms.
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.
