Fragile X Syndrome (FMR1 Repeat Analysis)
Test Code: GEN019 | Sample: Whole Blood (EDTA)
Test Overview
Genetic test that looks for inherited or acquired DNA changes linked to this condition. Fragile X Syndrome (FMR1 Repeat Analysis). Method: Methylation PCR (MS PCR), Fragment analysis, Triplet Primed PCR.
Preparation Instructions
No fasting is needed. Please bring your doctor's request form; genetic counselling before and after testing is recommended.
Sample Collection
A blood sample is drawn from a vein in your arm into a purple-top (EDTA) tube. Sample requirement: 3-5 ml of EDTA whole blood required. Sample stable for 3 Days at Amibent Temperature and 7 Days at 2 to 8 degree celsius. Clinical/family history, referring clinicians contact number and TRF mandatory.
About Your Results
Results are usually ready within 6 working days of the sample reaching the lab. You will be notified when your report is released, and you can download it from your patient portal.
Standard Clinical Reference Ranges
| Parameter Name | Normal Reference Range | Unit |
|---|---|---|
| Biological reference interval provided on official report. | ||