Test Price
2,800 AED✅ Home Collection Available
DPM3 Gene CDG Type 1O (NGS) Genetic Test in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل جين DPM3 لاضطراب الغلكزة الخلقي من النوع 1O (CDG1O) في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑Certified NGS Processing.
- Premium Logistics: Paid Hospital‑Grade Home Collection with ISO Cold‑Chain Transport & VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post‑Test Clinical Interpretation Support Included.
- Insurance Support: Direct Billing Verification via WhatsApp +971 54 548 8731.
ملخص طبي: يضمن هذا الفحص الجيني المتطور تشخيصًا دقيقًا لاضطراب الغلكزة الخلقي من النوع 1O باستخدام تقنية التسلسل الجيني من الجيل التالي (NGS) تحت إشراف نخبة من الأطباء المتخصصين، مع خدمة السحب المنزلي وخدمة استشارة ما بعد الفحص.
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.
(Arabic: يقدم تحليل جين DPM3 تشخيصًا جزيئيًا قاطعًا لاضطراب الغلكزة الخلقي النوع 1O، وهو مرض استقلابي وراثي نادر.)
| 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 | 2026 DHA/MOHAP Standards, ISO 9001:2015 | May Vary |
Physician Insight & Safety Protocol
“As a clinician, 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.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠ Medication Warning: 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
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.
يقوم هذا الاختبار بتسلسل جين DPM3 كاملاً للكشف عن الطفرات المسببة لاضطراب الغلكزة الخلقي من النوع 1O، وهو مرض استقلابي نادر.
How long does it take, and what sample is required?
The test requires 3 to 4 weeks from sample receipt, and we accept whole blood, extracted DNA, or a single drop on an FTA card.
يستغرق الاختبار من 3 إلى 4 أسابيع من استلام العينة، ونقبل عينة دم كامل، أو حمض نووي مستخلص، أو قطرة دم واحدة على بطاقة FTA.
Can I have the if I don’t have symptoms?
Individuals with a family history of CDG type 1O may pursue carrier screening after a genetic counselling session.
يمكن للأشخاص الذين لديهم تاريخ عائلي للإصابة بـ CDG النوع 1O إجراء اختبار الكشف عن الحامل بعد جلسة استشارة وراثية.
This service adheres to UAE Federal Decree-Law No. 41 of 2024 (Art. 87) on genetic testing, the UAE Child Rights Law (CDS Law 2026) for minors’ consent, and the UAE Personal Data Protection Law (PDPL). All data processed under ISO 9001:2015 Cert: INT/EGQ/2509DA/3139.
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All reports reviewed by DHA-Certified physicians