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Because of the lyonization, inactivation, and formation of Barr bodies in all female cells, only one X chromosome is active at any time.

Thus, triple X syndrome most often has only mild effects or has no effects.

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The first published report of a woman with a 47, XXX karyotype was by Patricia A. at Western General Hospital in Edinburgh, Scotland, in 1959.

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This hot babe with the honey-colored hair is very sophisticated looking. This gorgeous lady has big tits, a succulent red mouth and long beautiful fingers tipped ...Triple X syndrome can be diagnosed prenatally through amniocentesis or chorionic villus sampling.In Denmark, between 19, 76% of the prenatally diagnosed fetuses with triple-X were aborted. With improved information, the number of abortions diminished.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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Triple X syndrome can be diagnosed prenatally through amniocentesis or chorionic villus sampling.

In Denmark, between 19, 76% of the prenatally diagnosed fetuses with triple-X were aborted. With improved information, the number of abortions diminished.

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.

Because the vast majority of triple X females are never diagnosed, it may be very difficult to make generalizations about the effects of this syndrome.