Test Price
2,800 AED✅ Home Collection Available
CD3D Gene Immunodeficiency Type 19 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CD3D لنقص المناعة النوع 19 بتقنية التسلسل الجيني (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary / ملخص تنفيذي
- Precision Guarantee / ضمان الدقة: 99.9% Diagnostic Sensitivity via ISO-Accredited Processing. حساسية تشخيصية 99.9% عبر معالجة معتمدة بمعيار ISO.
- Premium Logistics / خدمات النقل المتميزة: Hospital-Grade Home Collection (8 AM–11 PM) with ISO-Certified Cold Chain & VIP Mobile Phlebotomy. سحب منزلي بمستوى المستشفيات عبر سلسلة تبريد معتمدة ISO وخدمة الفصد المتنقلة.
- Clinical Guidance / التوجيه السريري: Complimentary Telephonic Post-Test Clinical Guidance for Result Interpretation. استشارة سريرية هاتفية بعد الفحص لتفسير النتائج.
- Insurance / التأمين: Direct Billing Verification via WhatsApp +971 54 548 8731. تحقق من تغطية التأمين عبر واتساب.
Comprehensive NGS-Based CD3D Mutation Analysis
CD3D gene sequencing detects pathogenic variants responsible for primary immunodeficiency type 19 (SCID-like disorders), enabling early targeted interventions. يستخدم هذا التحليل المتقدم تقنية التسلسل الجيني الشامل لتحديد الطفرات المسببة لنقص المناعة الأولي النوع 19.
| Feature | Our NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | >99.9% analytical sensitivity for CD3D full coding region | ~99% – limited to exonic hotspots |
| Methodology | Next Generation Sequencing (NGS) with CNV detection | Sanger sequencing – single amplicon analysis |
| Turnaround Speed | 3–4 Weeks (comprehensive report with clinical annotation) | 4–6 Weeks (separate deletion/duplication assays required) |
Physician Insight & Safety Protocol
“Genetic testing for immunodeficiency can bring uncertainty, but knowledge empowers you. This NGS panel identifies CD3D mutations with remarkable accuracy; however, results must be correlated with your clinical history and family pedigree. I encourage you to share the findings with a clinical immunologist for a holistic interpretation.” — Dr. PRABHAKAR REDDY (DHA License: 61713011)
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your treating doctor. Genetic results complement, but never replace, clinical management.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: This non‑urgent genetic test is not suitable for individuals with acute life‑threatening infections, unstable vital signs, or those unable to provide informed consent. Pre‑test genetic counselling is mandatory; sample collection may be deferred if the patient is clinically unstable.
- ER Red Flags – seek immediate medical attention if you experience:
- Sudden high fever (>39°C) with rigors.
- Progressive respiratory distress or stridor.
- Signs of anaphylaxis (swelling of lips/tongue, severe urticaria).
- New‑onset confusion or loss of consciousness.
Frequently Asked Questions
1. What is the CD3D Gene Immunodeficiency Type 19 NGS test and why is it important?
Snippet: The CD3D Genetic Test diagnoses primary immunodeficiency type 19 by identifying harmful gene variants.
The test reads the entire CD3D gene using next‑generation sequencing to pinpoint single‑nucleotide changes, deletions, or duplications. Early diagnosis allows for tailored clinical surveillance, prophylactic antibiotics, or consideration of hematopoietic stem cell transplantation.
الملخص: يكشف تحليل جين CD3D بتقنية التسلسل الجيني الطفرات المسببة لنقص المناعة النوع 19 بدقة فائقة. يساعد التشخيص المبكر في توجيه الرعاية الوقائية والعلاج المناسب مثل زراعة الخلايا الجذعية.
2. What sample types are accepted and how should I prepare?
Snippet: We accept whole blood, extracted DNA, or one drop of blood on an FTA card—no fasting required.
A certified phlebotomist collects the sample during home visit (8 AM to 11 PM). Whole blood in EDTA tube is preferred; DNA must be extracted under sterile conditions. Provide a detailed clinical history and, if possible, a family pedigree from a pre‑ genetic counselling session.
الملخص: نقبل عينة دم كامل أو حمض نووي مستخلص أو قطرة دم على بطاقة FTA — ولا يشترط الصيام. يجب تقديم التاريخ السريري ومخطط شجرة العائلة قبل الفحص.
3. How are the results reported and what do they mean for my family?
Snippet: The report classifies variants as pathogenic, likely pathogenic, or VUS with clinical correlation, empowering cascade testing in relatives.
Results are issued in a physician‑friendly PDF with ACMG/AMP classification. A genetic counsellor explains the findings via a complimentary tele‑consultation. If a disease‑causing variant is found, first‑degree relatives can undergo targeted testing, enabling predictive counselling and early intervention.
الملخص: يصنف التقرير الطفرات حسب المعايير العالمية (ACMG) مع شرح سريري ويوصى بفحص الأقارب من الدرجة الأولى للكشف المبكر عن الحالة.
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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
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