Introducing
Your new presentation assistant.
Refine, enhance, and tailor your content, source relevant images, and edit visuals quicker than ever before.
Trending searches
Triple X syndrome may not cause any signs or symptoms. If symptoms do appear, they may include:
The mother's egg cell or the father's sperm cell has not formed correctly, resulting in an extra X chromosome. This random error in egg or sperm cell division is called nondisjunction.
It is a random mutation inherited by the mother. A genetic mutation.
This disease is only found in females. And it is in every 1 out of 1000 females on earth is diagnosed with this disease.
Triple X syndrome is not a inherited disease, but usually occurs as an event during the formation of reproductive cells (ovum and sperm). With an error in cell division called nondisjunction it can result in a reproductive cells with additional chromosomes.
Most Triple X females are never diagnosed, useless it is found later on in life through tests. Blood test are a way to diagnose this syndrome, because you can look at a persons chromosomes.
No known treatment
"Degree." Degree. N.p., n.d. Web. 26 Mar. 2014.
"Triple X Syndrome." Wikipedia. Wikimedia Foundation, 15 Mar. 2014. Web. 25 Mar. 2014.
"University of Michigan Health System." Triple X (XXX) Syndrome: Your Child:. N.p., n.d. Web. 26 Mar. 2014.
"Hanging Naked from the Garage Door." Single Dad Laughing. N.p., n.d. Web. 26 Mar. 2014.