Symptoms Signs and symptoms can vary greatly among girls and women with triple X syndrome. Some may experience no noticeable effect. Others may have mild symptoms. Occasionally significant symptoms may occur. Causes Although triple X syndrome is genetic, it's usually not inherited — it's due to a random genetic error. Normally, people have 46 chromosomes in each cell, organized into 23 pairs, which includes two sex chromosomes.

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One set of chromosomes is from the mother and the other set is from the father. These chromosomes contain genes, which carry instructions that determine everything from height to eye color. Hitachi 250gb External Hard Drive Drivers. The pair of sex chromosomes — either XX or XY — determines a child's sex. A mother can give the child only an X chromosome, but a father can pass on an X or a Y chromosome: • If the child receives an X chromosome from the father, the XX pair makes the child genetically a female.

• If the child receives a Y chromosome from the father, the XY pair means the child is genetically a male. Females with triple X syndrome have a third X chromosome from a random error in cell division. This error can happen before conception or early in the embryo's development, resulting in one of these forms of triple X syndrome: • Nondisjunction. In most cases, either the mother's egg cell or the father's sperm cell divides incorrectly, resulting in an extra X chromosome in the child. This random error is called nondisjunction, and all the cells in the child's body will have the extra X chromosome. Occasionally, the extra chromosome results from an incorrect cell division caused by a random event early in the embryo's development.

If this is the case, the child has a mosaic form of triple X syndrome, and only some cells have the extra X chromosome. So females with the mosaic form may have less obvious symptoms. Triple X syndrome is also called 47,XXX syndrome because the extra X chromosome results in 47 chromosomes in each cell instead of the usual 46. Complications Although some females may have no or mild symptoms associated with triple X syndrome, developmental delays or learning disabilities often occur and may lead to a variety of other issues, including: • Work, school, social and relationship problems • Anxiety and other emotional problems, such as attention-deficit/hyperactivity disorder (ADHD) and autism symptoms • Behavior problems • Poor self-esteem • Need for additional assistance with learning, activities of daily living, school or work. • Triple X syndrome. Genetics Home Reference. Accessed Sept.

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National Organization for Rare Disorders. Accessed Sept.

• Triple X syndrome. Merck Manual Consumer Version.

Accessed Sept. Photofunia New Effects 2012 For Pc more. • Van Rijn S, et al. The social behavioral phenotype in boys and girls with an extra X chromosome (Klinefelter syndrome and trisomy X): A comparison with autism spectrum disorder. Journal of Autism and Developmental Disorders. • Otter M, et al. Triple X syndrome: A review of the literature. European Journal of Human Genetics.

• Van Rijn S, et al. Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX. Genes, Brain and Behavior. • Hoecker JL (expert opinion). Mayo Clinic, Rochester, Minn. Dayz Mta Server on this page. • Pichurin PN (expert opinion). Mayo Clinic, Rochester, Minn.