Test Price
2,800 AED✅ Home Collection Available
FLNC Gene Filaminopathy Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection from 8 AM to 11 PM daily, with dedicated DHA-licensed courier handling.
- Clinical Guidance: Complimentary telephonic post‑test clinical guidance with a DHA‑licensed consultant medical geneticist.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The FLNC Gene Filaminopathy Genetic Test screens the entire coding region and splice junctions of the FLNC gene for variants causing filaminopathy‑related neurological and cardiac myopathies. This next‑generation sequencing assay delivers definitive molecular diagnosis for patients suspected of myofibrillar myopathy or restrictive cardiomyopathy.
| Feature | Our Test (NGS) | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Precision | Full gene coverage with copy number variant detection | Limited to selected exons; may miss deep intronic or CNV variants |
| Methodology | Next‑Generation Sequencing (Illumina® platform) + confirmatory Sanger | Sanger sequencing of one exon at a time |
| Turnaround Time | 3 – 4 Weeks | 8 – 12 Weeks (cumulative) |
Physician Insight & Safety Protocols
"Genetic results are a critical piece of the diagnostic puzzle. The FLNC NGS test pinpoints the molecular cause of muscle weakness or cardiomyopathy, but interpretation must integrate personal and family history. My team and I are available to guide you through your results within our clinical framework."
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue or adjust any prescribed medication without consulting your treating physician. Stopping cardiac or neurological drugs abruptly can trigger life‑threatening arrhythmias or acute muscle decompensation.
Exclusion Criteria & Emergency Red Flags
- Not suitable for individuals who have received whole blood transfusion within the last 7 days (donor DNA may interfere).
- If you experience sudden choking, difficulty swallowing, or unexplained fainting while awaiting results, proceed immediately to the nearest emergency department — these may signal an acute myopathic or cardiac crisis.
- This test requires a dedicated genetic counselling session prior to sample collection; do not collect a sample unless you have completed a counselling consult and pedigree chart.
Patient FAQ & Clinical Guidance
1. What does the FLNC NGS test detect, and why do I need it?
A: It identifies pathogenic variants in the entire FLNC gene that cause filaminopathy-related myofibrillar myopathy and restrictive cardiomyopathy, providing a definitive diagnosis for inherited muscle disease. Early molecular confirmation enables targeted cardiac surveillance and personalised treatment planning.
2. Can the sample be collected at home, and how do I receive results?
A: Yes, our DHA‑compliant mobile phlebotomy team visits your home between 8 AM – 11 PM using temperature-controlled cold-chain logistics. The final interpretive report is securely delivered via email in 3–4 weeks, with an optional tele‑counselling session.
3. Is the test covered by insurance in the UAE?
A: Many UAE insurers reimburse single‑gene NGS tests when medically indicated; contact our billing team on WhatsApp at +971 54 548 8731 for a free pre‑authorisation check and direct billing facilitation.
UAE Regulatory & Data Privacy Adherence
This laboratory complies with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL), Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, and Federal Decree‑Law No. 4 of 2016 on Medical Liability. Accredited under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). All genetic data is handled strictly on UAE‑based secure servers with role‑based access controls and audit logging.
Clinical & Logistical Metadata
| Test Name | FLNC Gene Filaminopathy Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 – 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (3–5 mL in EDTA tube) |
| Methodology Used | Next‑Generation Sequencing (Illumina®) with confirmatory Sanger sequencing |
| ICD-10-CM Code | G71.0, I42.8 |
| LOINC Code | 78014-3 |
| DHA Facility License & Laboratory Address | DHA Facility License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab Branding: DNA Labs UAE |
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians