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http://www.mayoclinic.org/diseases-conditions/triple-x-syndrome/symptoms-causes/dxc-20164623
https://en.wikipedia.org/wiki/Triple_X_syndrome

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XXX Syndrome is confirmed by a genetic testing and/or a blood sample to check the cells. however some people go their whole lives unknowing of the disesase because the symptoms may not be very serious.

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As of now, there is now way of permanently getting rid of this disease permanently, but certain medicine and a stable home environment can help improve symptoms.

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47 XXX Syndrome is not an inherited disease but rather occurs during the formation of reproductive cells. the extra X could come from either the mother or father.

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The most common symptoms for this disease is being taller than average, and an increased risk of learning disabilities and delayed development in motor skills. other symptoms include weak muscle tone, behavioral and emotional difficulties, seizures, and kidney abnormalities. only about 10% are affected by the more severe symptoms. however there are no prominent physical features about this disease.

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XXX Syndrome in not a super rare disease. It occurs in about 1 in 1000 newborn girls. Between 5 and 10 girls are born with this disease everyday in the U.S.

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The first known report of 47 XXX Syndrome was by a woman named Patricia A. Jacobs in 1959. She had her first symptom when she was 19 years old with a premature ovarian failure.

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Triple X syndrome is a disease caused by the presence of an additional X chromosome in female cells.