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Test Price

2,800 AED

✅ Home Collection Available

DPM3 Gene CDG Type 1O (NGS) Genetic Test in UAE | 2,800 AED | DHA Compliant

Executive Summary & Core Metrics

DHA‑Compliant ISO 9001:2015
  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑Certified NGS Processing.
  • Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily 8 AM – 11 PM).
  • Clinical Guidance: Telephonic Post-Test Clinical Interpretation Support Included.
  • Insurance Support: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

Comprehensive NGS Analysis for DPM3‑Related CDG Type 1O

The DPM3 gene NGS test provides a definitive molecular diagnosis for Congenital Disorder of Glycosylation Type 1O, a rare autosomal recessive metabolic disorder. By sequencing the entire coding region and detecting deletions/duplications, it pinpoints pathogenic variants with unmatched precision, enabling tailored medical management and informed genetic counselling.

Feature Our Test (DHA‑Listed Lab) Closest Alternative
Precision >99.9% Sensitivity & Specificity, Full Gene Coverage Sanger Sequencing of Single Exons; Misses Large Deletions
Method Next‑Generation Sequencing (Illumina platform), CAP/ISO validated Conventional PCR & Fragment Analysis
Turnaround 3–4 Weeks 6–8 Weeks
UAE Regulatory DHA/MOHAP Standards, ISO 9001:2015 May Vary

Physician Insight & Safety Protocols

“As a Consultant Medical Genetics, I understand that pursuing a genetic diagnosis can be an emotional journey. This test must be interpreted alongside the full clinical picture, including metabolic workup and family history, to ensure a comprehensive understanding. Please remember that a negative result does not exclude other forms of CDG, and genetic counseling is essential.”

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

Medication Advisory

⚠ Do not discontinue any prescribed medication without consulting your doctor.

Exclusion Criteria & Safety Red Flags

  • Recent blood transfusion (within 2 weeks) may affect DNA quality.
  • Active acute infection – postpone collection until resolved.
  • Inability to provide informed consent (guardian required for minors).
  • Emergency Red Flags: If you or your child experiences unexplained vomiting, lethargy, seizures, or loss of consciousness during the waiting period, seek immediate medical attention.

Patient FAQ & Clinical Guidance

1. What is the DPM3 gene CDG type 1O NGS test?

This test sequences the entire DPM3 gene to detect mutations causing Congenital Disorder of Glycosylation type 1O, a rare metabolic disease.

2. How long does it take, and what sample is required?

The test requires 3 to 4 weeks from sample receipt. We accept whole blood, extracted DNA, or a single drop on an FTA card. Home collection is available via our VIP Mobile Phlebotomy service.

3. Can I have the test if I don’t have symptoms?

Individuals with a family history of CDG type 1O may pursue carrier screening after a genetic counselling session.

UAE Regulatory & Data Privacy Adherence

This 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. Clinical safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. All genetic data is processed under strict confidentiality and ISO 9001:2015 certified quality management (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name DPM3 Gene CDG Type 1O (NGS) Genetic Test
Price (AED) 2,800 AED
Turnaround Time 3–4 Weeks
Sample Type / Matrix Whole blood, Extracted DNA, or FTA Card
Methodology Used Next-Generation Sequencing (Illumina Platform, CAP/ISO Validated)
ICD-10-CM Code E77.8
LOINC Code 81267-0
DHA Facility License & Laboratory Address DHA License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE

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