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Test Price

2,800 AED

✅ Home Collection Available

DNM2 Gene DI‑CMTB Next‑Generation Sequencing (NGS) Genetic Test in UAE | 2,800 AED

Executive Summary & Core Metrics

Accuracy & Logistics

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing (ISO 9001:2015 Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: VIP Mobile Phlebotomy & Temperature‐Controlled Cold‐Chain Home Collection – available daily 8 AM to 11 PM.
  • Post‑Test Guidance: Telephonic consultation with a consultant medical geneticist upon request.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The DNM2 Gene DI‑CMTB Genetic Test employs Next‑Generation Sequencing (NGS) to detect pathogenic variants in the DNM2 gene associated with Dominant Intermediate Charcot‑Marie‑Tooth disease type B. This molecular analysis provides definitive diagnosis and enables family risk stratification.

Feature Our Test (NGS) Closest Alternative (Single‑Gene Sanger)
Precision / Diagnostic Yield 99.9% sensitivity; full coding region coverage ~95% sensitivity; may miss deep intronic variants
Methodology Next‑Generation Sequencing (NGS) with bioinformatic analysis Sanger sequencing of targeted exons only
Turnaround Time 3–4 Weeks 6–8 Weeks (typical for reference labs)

Physician Insight & Safety Protocols

“As a consultant in medical genetics, I emphasize that this test should always be correlated with clinical and electrophysiological findings. Results provide powerful guidance for families, but a negative result does not exclude all genetic causes, and a positive result does not predict disease severity. Pre‑test genetic counselling is strongly advised.”

— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA ID: 9294403

Medication Advisory

Do not discontinue any prescribed medications without consulting your treating physician. This test is not a substitute for clinical evaluation.

Safety Exclusion Criteria & Emergency Red Flags

  • Exclusion Criteria: Individuals under 18 without legal guardian consent; specimens not meeting pre‑analytical requirements (e.g., degraded DNA).
  • Emergency Red Flags: Sudden severe muscle weakness, respiratory distress, or loss of ambulation. If any occur, seek immediate emergency evaluation—do not wait for test results.

Patient FAQ & Clinical Guidance

1. What is the DNM2 gene test for?

The DNM2 gene test identifies mutations causing Dominant Intermediate Charcot-Marie-Tooth disease type B, enabling accurate diagnosis and family screening. It is a definitive molecular test for this specific neuropathy.

2. How is the sample collected and what is the turnaround time?

Sample collection is performed via standard peripheral whole blood draw (EDTA) or saliva (Oragene DNA kit) through our VIP Mobile Phlebotomy service. Results are typically delivered within 3–4 weeks.

3. Do I need genetic counselling before this test?

Yes, pre‑test genetic counselling is mandatory to draw a detailed pedigree chart, discuss potential outcomes, and ensure informed consent. Our team can coordinate a telephonic session with a certified counsellor upon booking.

UAE Regulatory & Data Privacy Adherence

This laboratory service complies 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 handled with strict confidentiality and stored on secure, encrypted servers within the UAE.

Clinical & Logistical Metadata

Test Name DNM2 Gene DI‑CMTB Next‑Generation Sequencing (NGS) Genetic Test
Price (AED) 2,800 AED
Turnaround Time 3–4 Weeks
Sample Type / Matrix Peripheral whole blood (EDTA) or saliva (Oragene DNA kit)
Methodology Used Next‑Generation Sequencing (NGS)
ICD-10-CM Code G60.0
LOINC Code 21636-6
DHA Facility License & Laboratory Address DHA License 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE

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