Test Price
2,800 AED✅ Home Collection Available
COG6 Gene Glycosylation Disorder Type 3 Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
Diagnostic Precision & Service Highlights
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM–11 PM)
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731
Test Overview & Methodology
The COG6 Gene Genetic Test identifies pathogenic variants in the COG6 gene responsible for Congenital Disorder of Glycosylation Type 3 (CDG Type 3), an autosomal recessive metabolic disorder with multisystem involvement. Our platform uses Next Generation Sequencing (Illumina) to achieve full gene coverage, detecting SNVs, indels, and CNVs with high sensitivity.
| Feature | Our Test (NGS) | Closest Alternative |
|---|---|---|
| Precision | Full gene coverage, detection of SNVs, indels, CNVs | Sanger sequencing – limited to known hotspots |
| Method | Next Generation Sequencing (Illumina platform) | Capillary electrophoresis / single-exon walking |
| Speed | 3–4 Weeks | 6–8 Weeks (for full gene coverage) |
Physician Insight & Safety Protocols
“A COG6 mutation result must be interpreted alongside clinical symptoms such as hypotonia, seizures, and liver dysfunction. I advise families to view this test as a starting point for a comprehensive metabolic and neurological evaluation. A negative result does not exclude other glycosylation defects.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA ID: 9294403)
Advisory – Medication Safety
Medication Warning
Do not discontinue any prescribed medication without consulting your physician. This test does not replace ongoing clinical management.
Exclusion Criteria & Emergency Red Flags
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Acute febrile illness, inability to provide informed consent, severe coagulopathy.
- Exclusion: Refusal or non-attendance of genetic counselling session.
- 🚨 ER Red Flags: Sudden onset of vomiting, lethargy, hypoglycemia, new‑onset seizures, or acute hepatic decompensation – seek immediate medical attention.
Patient FAQ & Clinical Guidance
1. What conditions does the COG6 gene test detect?
This test detects pathogenic mutations in COG6 causing Congenital Disorder of Glycosylation Type 3, an inherited metabolic condition impacting multiple organs.
2. How is the test performed and how long does it take?
A simple blood draw or FTA card sample is sequenced using Next Generation Sequencing, with results delivered in 3 to 4 weeks. Home phlebotomy is available daily.
3. Does this require insurance pre‑approval?
Our team verifies coverage directly via WhatsApp at +971545488731, and home collection is available for insured and self‑pay patients alike.
UAE Regulatory & Data Privacy Adherence
Data Protection & Legal Compliance
This test and all associated patient data are handled in strict adherence to 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 consent protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | COG6 Gene Glycosylation Disorder Type 3 Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA), FTA Card, Extracted DNA – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection |
| Methodology Used | Next Generation Sequencing (Illumina) |
| ICD-10-CM Code | E77.8, Z82.79, Z13.228 |
| LOINC Code | 94146-5 |
| DHA Facility License & Address |
DHA License: 1143 Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE Corporate Lab: DNA Labs UAE |
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التحقق من التغطية التأمينية
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians