Prevention Genetics LogoExact Sciences is now Abbott
Test Code 558

Fragile X Syndrome via FMR1 CGG Repeat Expansion

FMR1

1 - 2 weeks (6 - 10 days STAT)

Need to add or remove a gene?

Who is this test for?
  • Individuals with relevant features who have a clinical or suspected diagnosis of Fragile X syndrome
  • Females with primary ovarian insufficiency before age 40 years
  • Males and females with features consistent with Fragile X-associated tremor/ataxia syndrome
  • Individuals with a family history of Fragile X syndrome
Method
Repeat-Primed PCR & MS-PCR
Specimen(s)

Blood, buccal, saliva

Order Options

OTHER OPTIONS
for standard institutional pricing.

Explore related tests

Questions? We can help.

Getting support has never been easier. Connect with our team for assistance with anything from test selection to interpreting results. Use the live chat button or visit our Contact us page.