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"Diagnose Triple X syndrome by having your doctor perform what's called a "heel test" on your newborn daughter. Typically conducted 24 to 48 hours after birth, a heel test consists of a blood sample taken from an infant's heel. The blood sample is screened for a wide variety of metabolic and genetic disorders, including Triple X syndrome."
Read more: How to Diagnose Triple X Syndrome | eHow.com http://www.ehow.com/how_2052189_diagnose-triple-x-syndrome.html#ixzz16iyC7Fwj
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Famous people who have triple x syndrome?
There are no famous individuals known to have Triple X syndrome (also called Trisomy X). Triple X syndrome is a genetic condition that affects females where they have an extra X chromosome (XXY) instead of the typical XX combination. It is a relatively rare condition and may often go undiagnosed.
Can you die from the triple x syndrome?
Triple X syndrome is not typically fatal and individuals with this condition usually have normal life expectancies. However, there may be an increased risk of certain health problems such as learning disabilities, delayed language development, and emotional issues. Regular medical check-ups and support can help manage any potential complications.
Does Triple X syndrome occur because of nondisjunction?
Yes, Triple X syndrome can occur due to nondisjunction during meiosis, resulting in an individual having an extra X chromosome (47, XXX) instead of the typical two X chromosomes (46, XX). Nondisjunction can happen during either the mother's or father's gamete formation.
What part of the body does triple x syndrome affect?
Triple X syndrome affects females and is caused by the presence of an extra X chromosome. This genetic condition can lead to mild to moderate intellectual and developmental delays, as well as tall stature and some physical differences. It may also affect reproductive system development and function.
What is a genetic disorder that can be detected by karyotyping?
Down's syndrome is one that can be detected, in this disorder the person has one extra chromosome. This chromosome failed to separate during cell divisoin which resulted in a gamete having 24 chromosomes instead of 23. A person with downs syndrome has 47 chromosomes which can be observed by karyotyping.Another in turner's syndrom, in only occurs on the X chromosome and it results in a female missing or having an abnormal X chromosome. In karyotyping you will see that the female only has one X chromosome. It can not occur in males because they only have one X chromosome and a Y chromosome can not survive by it self.Klinefelter's Syndrome is when a male has an extra X chromosome. So he will have XXY (47 chromosomes) this is also detected in karyotyping.Karyotyping is a test to examine chromosomes in a sample of cells, which can help identify genetic problems. They can also be used to study chromosomal aberrations, cellular function, and gather information past evolutionary events.
Can triple x syndrome inherited?
No. Triple X occurs on the sex chromosomes.
Do any famous people have triple x syndrome?
Patricia Ann Jacobs(1934-)has Triple X Syndrome. She is the first lady diagnosed Triple X. She is studying genetics now.
How do you prevent triple x syndrome?
abstinance
How is Fragile X syndrome detected?
By a DNA blood sample
What Triple x syndrome occurs because?
Nondisjunction
Is Turner's syndrome the same as triple x syndrome?
No, they are two different things. Normally, a woman has 46 X chromozomes. If there are only 45 of them, it´s the Monozomy X, so called Turner syndrome. If there are 47 of them, it´s the Trizomy X, also known as the Triple X syndrome.
What chromosomes carry triple x syndrome?
chromosome 21
Famous people who have triple x syndrome?
There are no famous individuals known to have Triple X syndrome (also called Trisomy X). Triple X syndrome is a genetic condition that affects females where they have an extra X chromosome (XXY) instead of the typical XX combination. It is a relatively rare condition and may often go undiagnosed.
Is there a treatment for Triple X Syndrome?
i dont think so but there might eventually. the above response is incorrect. Triple X syndrome does not have a treatment because you cannot take an X chromosome away from every cell in the body
How does triple x syndrome occur?
Triple X syndrome is a genetic disorder in which a girl has three X chromosomes instead of two. Triple X occurs once in every 1,000 female births. However, doctors believe many girls with Triple X go their lifetime undiagnosed. The major features of Triple X are learning, behavioral and emotional problems. Compared with other syndromes in which a person has inherited three chromosomes. Triple X is quite mild in nature.
Is triple x syndrome race or gender centered?
Gender. Only Females can get it.
What gene is triple x syndrome?
it is on gene 8 the gene name is RECQL4
