Answers.com > Wiki Answers > Categories > Health > Conditions and Diseases > How is triple x syndrome diagnosed?

How is triple x syndrome diagnosed?

In: Conditions and Diseases, Genetics [Edit categories]

Answer:

Blood is drawn and genetic testing is done. It takes time. The blood is sent to a special lab.

First answer by Pegalita. Last edit by Pegalita. Contributor trust: 142 [recommend contributor ]. Question popularity: 2 [recommend question].

[report abuse]

Can you answer these Conditions and Diseases questions?

	Can anyone take insulin?	Answer it!
	What are symptoms of a brain tumor?	Answer it!
	What is a pedal stool?	Answer it!
	How do you get rid of an chronic ear infection on a English Mastiff?	Answer it!
	What does low MPV and high MCH mean?	Answer it!

Can you die from the triple x syndrome?
No, you can not die from Triple X syndrome. Your are going to live a normal life .
What gene is triple x syndrome?
it is on gene 8the gene name is RECQL4
How is Triple X syndrome detected?
"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...
When is fragile x syndrome diagnosed?
Fragile X can be diagnosed at any time, at 1 month, 2 years, 10 years, 40 years or 70 years. It can be diagnosed prior to birth through amnio or cvs. When testing for fragile x it is important that...
Can Triple X syndrome be cured?
No it can not be cured