Origin of Discovery Triple x syndrome was discovered in 1959 by Patricia Jacobs who worked in a hospital in Scotland. She discovered it from a 35 year old woman, who had undergone Premature Menopause. They found that it was caused by having an extra x chromosome in a female. Many doctors say that many women will never be diagnosed because sometimes, some symptoms can never be noticeable. …show more content…
They can have a vertical fold of skin that goes across the inner angle of an eye. In very rare cases reproductive issues can occur like menstural irregularities, early mensstruation, and sometimes infertility. There are some cases where they can have curved pinkey fingures, early or late puberty, constipation, abdomal pains, frequent urinary tract infections, and flat feet. They can also have heart abnormalities, abnormally shaped breastbone, memory judgment, and information processing problems (Mayoclinic.org)
How many and who gets it? Triple x Syndrome can only affect females. The reason that it can only affect females is because men need to have a Y chromosome. The likelihood of a person getting it is one in 900 to 1,000 births. It can happen to every female, but it is not that common. Many women may never be diagnosed because some symptoms are not noticeable or there are none (NORD.org).
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