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Triple X syndrome is not inherited, but usually occurs as an event during the formation of reproductive cells ovum and sperm. Triple X syndrome occurs in around 1 in 1, girls. English translation from original Dutch by Jill Balfour. Triple X syndrome , also known as trisomy X and 47,XXX , is characterized by the presence of an extra X chromosome in each cell of a female. Epicanthal folds and increased distance between the eyes in 2-year-old girl with trisomy X [2].

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Females with triple X syndrome often have delayed language development. Orphanet Journal of Rare Diseases. Institute , Sacramento, California. A stable home environment can improve some of the symptoms.

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