Test Price
2,800 AED✅ Home Collection Available
COG7 Gene Congenital Disorder of Glycosylation Type IIe (CDG‑IIe) Genetic Test in UAE | AED 2,800 | DHA Licensed
Executive Summary & Core Metrics
99.9% Diagnostic Sensitivity
NGS with full exon coverage and CNV analysis, processed in our ISO 9001:2015‑accredited laboratory.
VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection
Available daily from 8 AM to 11 PM, all emirates. DHA‑licensed professionals ensure painless collection with clinical‑grade cold chain.
Post‑Test Clinical Guidance
Free telephonic interpretation of results with a DHA‑certified physician to clarify clinical implications and metabolic management.
Direct Insurance Billing
Instant eligibility check and pre‑approval verification via WhatsApp at +971 54 548 8731.
Accuracy Guarantee: Diagnostic sensitivity of 99.9% through ISO‑accredited processing. Premium home collection with cold‑chain transport. Free telephone medical consultation after result delivery. Insurance verification via WhatsApp.
Test Overview & Methodology
This genetic test screens the entire coding region of the COG7 gene for pathogenic variants causing Congenital Disorder of Glycosylation Type IIe (CDG‑IIe), a severe multisystem metabolic condition. Using Next‑Generation Sequencing (NGS) with copy number variation (CNV) analysis, it delivers a definitive molecular diagnosis to guide early intervention, metabolic management, and family planning.
| Feature | Our COG7 NGS Test | Standard Genetic Panel |
|---|---|---|
| Diagnostic Precision | 99.9% analytical sensitivity for COG7 full CDS ± 20 bp | 95–97% coverage, may miss deep‑intronic variants |
| Methodology | NGS + integrated CNV detection (MLPA confirmatory) | Sanger sequencing or limited NGS sub‑panel |
| Turnaround Time | 3–4 weeks (expedited reporting available) | 6–8 weeks (whole exome/genome) |
| Clinical Reporting | DHA‑guided interpretation, metabolic specialist review | Generic variant‑only report |
Physician Insight & Safety Protocols
“As a consultant medical geneticist with deep expertise in inborn errors of metabolism, I recognize the anxiety a parent feels when pursuing a diagnosis for a child with developmental delay. The COG7 NGS test provides a precise molecular answer, enabling early metabolic management and accurate genetic counselling. Please remember that a positive result must be correlated with biochemical findings and clinical phenotype.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Important Advisory
Do not discontinue any prescribed medication or dietary supplement without explicit consultation with your treating physician. Genetic information alone does not replace ongoing clinical management. Always follow the metabolic and dietary recommendations of your specialist.
Safety Exclusion Criteria & Red Flags
- Exclusion from home collection: Active febrile illness >38.5 °C, acute bleeding disorder, or severe dehydration — hospital sampling advised.
- Emergency warning signs: If the patient develops sudden lethargy, intractable vomiting, hypoglycaemia, or seizures, proceed to the nearest ER immediately. This test is not a tool for acute crisis management.
- Minors: In compliance with Federal Decree‑Law No. 4 of 2016 on Medical Liability, a legal guardian must provide informed consent and be present during sample collection.
Patient FAQ & Clinical Guidance
1. How accurate is this COG7 genetic test for confirming CDG‑IIe?
This NGS test identifies >99.9% of single nucleotide variants and exonic deletions in COG7 with full analytical validation, making it the definitive molecular confirmation for Congenital Disorder of Glycosylation Type IIe.
2. What sample types are accepted and how is the collection done?
A single blood sample (3–5 mL in EDTA), extracted DNA, or a dried blood spot on an FTA card are all suitable. Our DHA‑licensed phlebotomist arrives at your home with full cold‑chain equipment for a painless collection. VIP Mobile Phlebotomy is available daily from 8 AM to 11 PM across all emirates.
3. How long do results take and what does the report include?
Results are delivered in 3–4 weeks with a comprehensive report detailing variant classification, zygosity, and clinical significance, accompanied by a free post‑test consultation to discuss implications and metabolic management.
4. Will my health insurance cover this test?
We offer direct insurance billing with instant eligibility checks. Send your policy details via WhatsApp at +971 54 548 8731 for quick pre‑approval verification.
UAE Regulatory & Data Privacy Adherence
This test is performed in full compliance with UAE federal laws:
- Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) – ensuring strict confidentiality and secure handling of your genetic data.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – governing secure electronic health records and telemedicine.
- Federal Decree‑Law No. 4 of 2016 on Medical Liability – ensuring informed consent and safe clinical practices for minor patients.
Our laboratory is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139). The DHA Facility License and physical address are listed in the metadata below.
Clinical & Logistical Metadata
| Test Name | COG7 Gene Congenital Disorder of Glycosylation Type IIe (CDG‑IIe) Genetic Test |
| Price (AED) | AED 2,800 |
| Turnaround Time | 3–4 weeks (expedited reporting available) |
| Sample Type / Matrix | Whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) |
| Methodology Used | Next‑Generation Sequencing (NGS) with copy number variation (CNV) analysis |
| ICD-10-CM Code | E77.8 |
| LOINC Code | 21636-6 |
| DHA Facility License & Laboratory Address Invariants | DHA Facility License Number: 1143 Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE Corporate Lab Branding: DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians