Triple X syndrome is not inherited, but usually, occurs as an event during the formation of reproductive cells (ovum and sperm).

An error in cell division called nondisjunction can result in reproductive cells with additional chromosomes.

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In some cases, trisomy X occurs during cell division in early embryonic development.

Some females with triple X syndrome have an extra X chromosome in only some of their cells. The vast majority of triple X women are never diagnosed, unless they undergo tests for other medical reasons later in life.The symptoms vary from person to person, with some women being more affected than others.Symptoms may include tall stature, vertical skin folds that may cover the inner corners of the eyes (epicanthal folds), poor muscle tone, and a curve in the 5th finger towards the 4th.Posted: , Author: Vimuj Offering exclusive content not available.Thousands of happy men and women have met their soul mates on Malaysian Cupid and have shared their stories with.Triple X can be diagnosed by a blood test which is able to look at a person’s chromosomes (karyotype).