Test Price
2,800 AED✅ Home Collection Available
CWF19L1 Gene Spinocerebellar Ataxia Type 17 (Autosomal Recessive) Genetic Test
Executive Summary & Core Metrics
At a Glance
- Diagnostic Precision: 99.9% analytical sensitivity via ISO 9001:2015‑certified processing, ensuring reliable genetic diagnosis for autosomal recessive spinocerebellar ataxia type 17.
- Premium Logistics: VIP mobile phlebotomy and temperature‑controlled cold‑chain home collection available daily from 8 AM to 11 PM across all UAE emirates.
- Clinical Guidance: Post‑test telephonic consultation for result interpretation by DHA‑licensed medical geneticists and neurologists.
- Insurance Facilitation: Direct billing verification and pre‑authorization support via WhatsApp at +971 54 548 8731, in compliance with UAE health insurance regulations.
Test Overview & Methodology
This clinically validated Next‑Generation Sequencing (NGS) test screens the entire coding region of the CWF19L1 gene for pathogenic variants linked to autosomal recessive spinocerebellar ataxia type 17 (SCA17). Delivering 99.9% analytical sensitivity, it is processed in our ISO 9001:2015‑certified laboratory, fully aligned with Dubai Health Authority genetic diagnostic standards. Results include comprehensive variant interpretation and are returned within 3–4 weeks.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision / Methodology | Full‑gene NGS with Sanger confirmation; detects single nucleotide variants, small indels, and copy number changes | Targeted mutation panel (limited to known hotspots only) |
| Turnaround Time | 3–4 weeks (express option available) | 6–8 weeks (often outsourced abroad) |
| Regulatory Compliance | DHA / MOHAP guidelines, UAE PDPL, Federal Law No. 2 of 2019, ISO 9001:2015 | Variable; data sovereignty and consent may not meet UAE standards |
Physician Insight & Safety Protocols
Mrs. Lina Osama Zaki Quteineh (Consultant Medical Genetics, DHA Registration ID: 9294403) advises: “SCA17 is a progressive neurodegenerative condition; genetic diagnosis allows families to understand prognosis, enroll in research, and plan future healthcare. However, results must always be correlated with clinical findings and imaging. I strongly urge all patients and at‑risk relatives to complete pre‑ and post‑test genetic counseling—it transforms raw data into meaningful, actionable insight.”
Safety Advisory: Sample Collection & Clinical Context
This test uses standard peripheral whole blood, saliva, or buccal swab specimens. Our VIP mobile phlebotomy service is available for home collection under temperature‑controlled cold‑chain conditions. Patients on anticoagulant therapy should consult their physician before blood draw; alternative sample types (saliva or buccal swab) can be discussed as appropriate.
Exclusion Criteria & Emergency Red Flags
- Acute neurological decompensation (e.g., sudden ataxia worsening, inability to walk, dysphagia with aspiration) warrants immediate emergency department evaluation, not elective genetic testing.
- Known intractable coagulopathy or current therapeutic anticoagulation that cannot be safely withheld may contraindicate blood draw; in such cases, discuss use of saliva or buccal swab as alternative sample types.
- If you experience severe headache, visual disturbances, loss of consciousness, or seizures, proceed to the nearest ER and inform staff about the ongoing genetic work‑up.
Patient FAQ & Clinical Guidance
1. What is the diagnostic accuracy of this CWF19L1 NGS test?
We achieve over 99.9% analytical sensitivity and specificity by sequencing the entire coding region of CWF19L1 using NGS with orthogonal confirmation of all pathogenic variants.
2. How can I schedule home sample collection in the UAE?
Simply contact our WhatsApp support at +971 54 548 8731 to arrange a paid, hospital‑grade home phlebotomy service; we operate 8 AM – 11 PM daily, with cold‑chain transport to our ISO‑certified lab.
3. Is this genetic test covered by UAE health insurance?
We provide direct billing verification via WhatsApp; many UAE insurers cover medically necessary genetic diagnostics for spinocerebellar ataxia when ordered by a DHA‑licensed neurologist or clinical geneticist, and we assist with pre‑authorization.
4. What is the turnaround time for results?
Results are typically available within 3–4 weeks from sample receipt. An express option is available upon request for an additional fee.
5. Will I receive genetic counseling with my results?
Yes, we provide a post‑test telephonic consultation with a DHA‑licensed medical geneticist to help interpret your results and discuss implications for you and your family.
UAE Regulatory & Data Privacy Adherence
All patient data and genetic information remain within UAE boundaries, processed in compliance 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. A legally valid informed consent is mandatory before initiating testing, as per Federal Decree‑Law No. 4 of 2016 on Medical Liability and DHA genetic testing regulations. Clinical safety and patient consent procedures adhere strictly to UAE federal health data protection standards.
Clinical & Logistical Metadata
| Test Name | CWF19L1 Gene Sequencing – Autosomal Recessive Spinocerebellar Ataxia Type 17 (SCA17) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks (express option available) |
| Sample Type / Matrix | Whole blood (EDTA), saliva, or buccal swab – VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily (8 AM – 11 PM) |
| Methodology Used | Next‑Generation Sequencing (NGS) of full coding region with Sanger confirmation of pathogenic variants |
| ICD-10-CM Code | G11.9 (Spinocerebellar ataxia, unspecified) |
| LOINC Code | 82154-2 (Gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method) |
| DHA Facility License & Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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