Test Price
2,800 AEDโ Home Collection Available
FASTKD2 Gene โ Mitochondrial Complex IV Deficiency Genetic Test (NGS) in UAE | 2,800 AED
Executive Summary & Core Metrics
Clinical Executive Summary
- 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 (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Interpretation by DHA-Licensed Consultant Medical Geneticist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 (within 2 hours).
UAE Regulatory Compliance: 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; Federal Decree-Law No. 4 of 2016 on Medical Liability.
DHA Facility License: 1143 | Support: +971 54 548 8731 (WhatsApp 24/7).
Test Overview & Methodology
The FASTKD2 Gene test leverages Next-Generation Sequencing (NGS) to detect pathogenic variants causing Mitochondrial Complex IV (Cytochrome c Oxidase) Deficiency โ a severe neurometabolic disorder with early-onset neurological decline. Designed for patients in the UAE, this definitive genetic analysis enables precise diagnosis, family cascade screening, and personalized therapeutic strategies under a robust DHA-compliant workflow.
| Feature | Our FASTKD2 NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision (Analytical Sensitivity) | >99.9% โ Deep coverage of entire coding region | ~95% โ Limited to selected exons |
| Methodology | Next Generation Sequencing (NGS) with CNV analysis | Capillary (Sanger) bidirectional sequencing |
| Turnaround Time | 3 โ 4 Weeks | 4 โ 6 Weeks |
| Variant Detection | SNVs, indels, deep intronic splice sites, large deletions/duplications | Mainly SNVs and small indels |
| Sample Flexibility | Blood, Extracted DNA, One-drop Blood on FTA Card | Whole blood or purified DNA |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
โMitochondrial disorders present a complex diagnostic challenge that often requires integration of biochemical, imaging, and molecular data. The FASTKD2 analysis provides a critical piece of this puzzle, but it must be interpreted within the full clinical context. I encourage patients and families to engage in thorough pre- and post-test genetic counselling to fully understand the implications of their results.โ
โ ๏ธ Critical Clinical Warning
Do not discontinue any prescribed medication, supplements, or mitochondrial cocktail therapy without explicit instruction from your treating physician. Abrupt cessation can precipitate metabolic decompensation.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Patients experiencing acute encephalopathic crisis or active seizure within 48 hours prior to collection.
- Minors: Must have documented informed parental consent; testing of asymptomatic minors without clinical justification is strongly discouraged.
- Anticoagulation: Individuals on high-dose anticoagulants (e.g., warfarin, heparin) require written clearance from the managing physician for venipuncture.
- Emergency Red Flags โ Seek Immediate Hospital Care, Not At-Home Testing: Sudden loss of consciousness, uncontrolled seizures, acute respiratory distress, or severe lactic acidosis symptoms.
Patient FAQ & Clinical Guidance
1. What is the FASTKD2 gene test and when is it indicated?
The FASTKD2 gene test definitively identifies pathogenic mutations in the FASTKD2 gene responsible for mitochondrial complex IV deficiency, a neurometabolic disorder. Clinical indications include unexplained neurological regression, failure to thrive, hypotonia, and suspected Leigh-like syndrome. It is often ordered by Consultant Neurologists or Clinical Geneticists after metabolic screening.
2. How is the sample collected and what is the wait time for results?
A simple blood draw, one-drop blood on an FTA card, or previously extracted DNA is collected via VIP Mobile Phlebotomy with temperature-controlled cold-chain logistics. The analysis requires 3โ4 weeks because of extensive sequencing, bioinformatic interpretation, and two-clinician validation. You will receive a secure, DHA-format report.
3. Is the FASTKD2 test covered by insurance in the UAE, and how do I confirm?
Direct billing verification is processed instantly when you share your policy details via WhatsApp at +971 54 548 8731. We collaborate with major UAE insurers; pre-authorization is completed within 2 hours, and you only pay the non-covered portion, if any.
UAE Regulatory & Data Privacy Adherence
Your genetic data is protected under 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. Clinical safety and patient consent procedures comply with Federal Decree-Law No. 4 of 2016 on Medical Liability. All test results are transmitted via encrypted channels, and no genetic information is shared with third parties without your explicit written consent.
Clinical & Logistical Metadata
| Test Name | FASTKD2 Gene โ Mitochondrial Complex IV Deficiency Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 โ 4 Weeks |
| Sample Type / Matrix | Whole Blood, Extracted DNA, or One-drop Blood on FTA Card |
| Methodology Used | Next-Generation Sequencing (NGS) with CNV Analysis |
| ICD-10-CM Code | E88.49 |
| LOINC Code | 94222-3 |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE |
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