Test Price
2,800 AED✅ Home Collection Available
CP Gene Cerebellar Ataxia NGS Genetic Test in Dubai | 2,800 AED | Accredited Molecular Diagnostics
Executive Summary & Core Metrics
99.9% Diagnostic Sensitivity via ISO 15189-accredited NGS processing and strict bioinformatics pipeline.
VIP Mobile Phlebotomy and Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
Post-test telephonic genetic counseling by DHA-licensed Consultant Medical Genetics specialist to interpret your result.
Direct insurance verification via WhatsApp +971 54 548 8731 — we handle the paperwork.
Test Overview & Methodology
This Next Generation Sequencing (NGS) panel analyzes the CP gene and other high-evidence genes linked to hereditary cerebellar ataxia, delivering a comprehensive molecular diagnosis for progressive balance and coordination disorders. The assay covers all coding exons, splice sites, and select deep intronic regions to maximize variant detection yield.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision | 99.9% analytical sensitivity and specificity | 95–98% single-gene Sanger sequencing |
| Methodology | NGS with CNV and deep intronic variant analysis | Sanger sequencing or limited gene panels |
| Turnaround | 3–4 Weeks | 6–12 Weeks send-out laboratories |
Physician Insight & Safety Protocols
“A definitive molecular diagnosis of hereditary cerebellar ataxia through a comprehensive NGS panel empowers patients and their families with actionable information for clinical management and reproductive planning. Every variant must be interpreted within the complete clinical context; rare missense changes often require family co-segregation analysis to establish pathogenicity.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory Medication Notice
⛔ Do Not Self-Adjust Treatment
Never discontinue, modify, or initiate any prescribed medication based solely on a genetic test result. Always consult your treating physician who can integrate genetic findings with your full medical history and current therapy regimen.
Exclusion Criteria & Emergency Red Flags
⛔ Clinical Contraindications
- This test is intended for individuals with a clinical suspicion of hereditary ataxia; it is not a general screening tool.
- If you are experiencing acute neurological deterioration, severe headache, or respiratory distress, seek emergency care immediately — do not delay for a genetic test.
- Minors require legal guardian consent and a pediatric neurologist referral in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
- For specimens collected on an FTA card, avoid contaminating the collection area with food, liquid, or direct touch; follow the provided kit instructions exactly.
ER Warning: Acute-onset gait loss, dysarthria with swallowing difficulty, or new-onset double vision warrants immediate emergency department evaluation.
Patient FAQ & Clinical Guidance
1. What does the CP gene cerebellar ataxia NGS test detect?
This comprehensive sequencing panel analyzes the entire coding region and flanking splice sites of the CP gene, together with other clinically validated ataxia-associated genes. It identifies point mutations, small insertions and deletions, and copy number variants that may underlie hereditary cerebellar ataxia.
2. How should I prepare for the home blood collection appointment?
No fasting is required, but staying well-hydrated is recommended. Continue all prescribed medications unless your physician instructs otherwise. A trained phlebotomist will collect 2–4 ml of whole blood into a specialized DNA-stabilizing tube during your scheduled home visit between 8 AM and 11 PM.
3. Will my insurance cover the 2,800 AED cost, and how might the result affect my family?
Many UAE insurance plans provide coverage for diagnostic genetic testing in neurodegenerative disorders; our dedicated team conducts eligibility verification and obtains pre-approval on your behalf. A positive finding may prompt cascade testing for at-risk biological relatives, which we can coordinate with strict confidentiality.
UAE Regulatory & Data Privacy Adherence
Data Protection & Legal Framework
DNA Labs UAE operates under strict 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. All genetic data is encrypted, access-controlled, and processed exclusively within the UAE jurisdiction. Clinical safety and patient consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.
Your genetic information is protected by the same legal standards governing medical confidentiality in the UAE. No data is shared with third parties without explicit written consent. Results are delivered through secure encrypted channels, and you retain full rights to access, rectify, or request deletion of your personal data under PDPL.
Clinical & Logistical Metadata
| Test Name | CP Gene Cerebellar Ataxia NGS Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA) or FTA Card — VIP Mobile Phlebotomy and Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM |
| Methodology Used | Next Generation Sequencing (NGS) with CNV and Deep Intronic Variant Analysis |
| ICD-10-CM Code | G11.9, G11.8, G11.0 |
| LOINC Code | 90206-2 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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