Test Price
1,800 AED✅ Home Collection Available
Fragile X (FMR1) Carrier Genetic Test in UAE
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Complimentary telephonic post-test clinical guidance session with our Consultant Medical Genetics.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
- Price: 1800 AED (includes home collection and genetic counseling).
Test Overview & Methodology
Sanger sequencing‑based Fragile X (FMR1) carrier testing detects CGG repeat expansions in the FMR1 gene with unmatched precision. This comprehensive genetic assessment accurately identifies carrier status for Fragile X syndrome, enabling informed reproductive planning.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Method | Sanger Sequencing (Gold Standard) | Triplet‑Repeat PCR + Capillary Electrophoresis |
| Turnaround Time | 12–15 days | 7–10 days |
| Sensitivity | 99.9% (full allele sizing) | 95–98% (premutation detection) |
| Price (AED) | 1800 | 1200–1500 |
Physician Insight & Safety Protocols
“As a consultant in medical genetics, I understand the concerns regarding carrier screening. A positive result indicates carrier status, not a diagnosis—it empowers you to make informed family planning decisions. Our team provides comprehensive genetic counseling and guidance at every step.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics | DHA Registration ID: 9294403
Advisory & Precautions
Do not discontinue any prescribed medication without consulting your doctor prior to this test. Inform your physician about all medications and supplements you are taking. A single blood draw is required using an EDTA tube.
Exclusion Criteria & Red Flags
- Individuals unable to provide informed consent (by self or legal guardian).
- Active acute illness requiring immediate medical intervention.
- If you experience chest pain, difficulty breathing, or altered consciousness, seek emergency care immediately before attempting sample collection.
- Recent blood transfusion (within 4 weeks) may interfere with DNA analysis.
Patient FAQ & Clinical Guidance
1. What does the Fragile X carrier test detect?
This test identifies CGG repeat expansions in the FMR1 gene that indicate carrier status for Fragile X syndrome. It allows accurate risk assessment for passing the mutation to offspring.
2. How is the sample collected and is home collection available?
A single blood draw (EDTA tube) is required. VIP Mobile Phlebotomy and temperature‑controlled cold‑chain home collection are available daily from 8 AM to 11 PM, ensuring sample integrity from your doorstep to our ISO‑certified lab.
3. When will I receive my results and how are they communicated?
Results are delivered within 12–15 business days, accompanied by a complimentary telephonic clinical guidance session with our Consultant Medical Genetics. A PDF report is shared via secure email or WhatsApp.
UAE Regulatory & Data Privacy Adherence
This test is conducted under DHA Facility License 1143. The laboratory complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent is obtained in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | Fragile X (FMR1) Carrier Test |
| Price (AED) | 1800 |
| Turnaround Time | 12–15 business days |
| Sample Type / Matrix | Whole Blood (EDTA tube) |
| Methodology Used | Sanger Sequencing (Gold Standard) |
| ICD-10-CM Code | Z13.71 |
| LOINC Code | 21780-5 |
| DHA Facility License & Address | License No: 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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All reports reviewed by DHA-Certified physicians