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Test Price

2,800 AED

✅ Home Collection Available

GDAP1 Gene CMT4A Genetic Test – Next Generation Sequencing (NGS) | 2800 AED

Executive Summary & Core Metrics

Executive Summary

The GDAP1 Gene CMT4A NGS test uses next-generation sequencing to detect pathogenic variants in the GDAP1 gene associated with Charcot-Marie-Tooth disease type 4A. The test provides 99.9% diagnostic sensitivity and includes telephonic post-test clinical guidance.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
  • Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available 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 GDAP1 Gene CMT4A NGS test screens for pathogenic variants in the GDAP1 gene causing Charcot-Marie-Tooth disease type 4A, a severe, early-onset hereditary motor and sensory neuropathy. This comprehensive genetic test supports accurate diagnosis for patients with hereditary neuropathy symptoms.

Test Attributes Our Test (GDAP1 NGS) Closest Alternative (Single‑Gene Sanger)
Precision Full gene coverage, deep intronic & regulatory variants detected by NGS Coding exons only; limited variant detection
Methodology Next Generation Sequencing (NGS) with copy number analysis Sanger sequencing (exon‑by‑exon, no CNV detection)
Turnaround Time 3‑4 Weeks 6‑8 Weeks
Sample Flexibility Whole Blood, Extracted DNA, or Dried Blood Spot (FTA® Card) Whole Blood only

Physician Insight & Safety Protocols

“While this genetic test identifies GDAP1 mutations linked to CMT4A, clinical correlation with neurological examination and family history is essential. A negative result does not exclude other genetic forms of Charcot-Marie-Tooth disease. Always discuss results with your neurologist.” – Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA ID: 9294403

Advisory Notice

Do not discontinue prescribed medication without consulting your doctor. Genetic results do not replace ongoing clinical management.

Exclusion Criteria & Red Flags

  • Not indicated for individuals without clinical suspicion of hereditary neuropathy or positive family history.
  • Requires a pre‑test genetic counselling session to document pedigree (mandatory).
  • 🆘 Seek immediate medical attention if you experience sudden muscle weakness, respiratory difficulty, severe neuropathic pain, or loss of ambulation.

Patient FAQ & Clinical Guidance

1. What is the GDAP1 gene and its role in CMT4A?

This NGS test sequences the entire GDAP1 gene to identify variants responsible for Charcot-Marie-Tooth disease type 4A, a severe autosomal recessive neuropathy.

2. How is the test performed and what sample is required?

A simple blood draw, one drop of blood on an FTA card, or previously extracted DNA is accepted. Home collection is available 8 AM–11 PM via our VIP mobile phlebotomy service.

3. Will insurance cover this genetic test?

Direct billing verification is offered via WhatsApp at +971 54 548 8731. Many UAE insurers cover medically necessary hereditary neuropathy panels.

UAE Regulatory & Data Privacy Adherence

All genetic testing services at DNA Labs UAE comply 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. Clinical testing safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name GDAP1 Gene CMT4A Genetic Test (NGS)
Price (AED) 2,800 AED
Turnaround Time 3–4 Weeks
Sample Type / Matrix Whole Blood, Extracted DNA, or Dried Blood Spot (FTA® Card)
Methodology Used Next Generation Sequencing (NGS) with Copy Number Variation (CNV) analysis
ICD-10-CM Code G60.0
LOINC Code 81252-4
DHA Facility License & Laboratory Address 1143 · Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE · DNA Labs UAE

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