Test Price
2,800 AED✅ Home Collection Available
MYD88 Gene Recurrent Pyogenic Bacterial Infections Due to MYD88 Deficiency Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين MYD88 للكشف عن العدوى البكتيرية القيحية المتكررة الناتجة عن نقص MYD88 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
✅ Diagnostic Accuracy: 99.9% Sensitivity via ISO 9001:2015 Certified NGS
🏠 Premium Logistics: Hospital‑Grade Home Collection (8 AM – 11 PM) with ISO‑Certified Cold‑Chain
📋 Clinical Guidance: Telephonic Post‑Test Genetic Counselling with DHA‑Licensed Physician
📞 Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731
فحص الجين MYD88 بتقنية التسلسل الجيني من الجيل التالي (NGS) يُشخّص نقص المناعة الوراثي النادر المسؤول عن عدوى بكتيرية قيحية متكررة. نضمن دقة تشخيصية 99.9% وسعر 2800 درهم مع خدمة سحب منزلي معتمدة من هيئة الصحة بدبي وفقًا للمرسوم بقانون اتحادي رقم 41 لسنة 2024. جميع البيانات محمية بموجب قانون حماية البيانات الشخصية الإماراتي.
Facility License: 9834453 | ISO 9001:2015 Cert: INT/EGQ/2509DA/3139 | All testing complies with UAE PDPL & Federal Decree‑Law No. 41 of 2024 (Art. 87).
Clinical Overview
The MYD88 Gene NGS Test analyses the entire coding region of the MYD88 gene to detect pathogenic variants causing MYD88 deficiency, an autosomal recessive primary immunodeficiency leading to recurrent, severe pyogenic bacterial infections. This advanced genetic test enables definitive diagnosis, guides targeted antibiotic prophylaxis and immunoglobulin therapy, and facilitates family screening for proactive healthcare management.
يقوم فحص MYD88 بتسلسل الجين الكامل للكشف عن الطفرات المسببة لنقص المناعة الوراثي الذي يؤدي إلى عدوى بكتيرية قيحية خطيرة ومتكررة، مما يتيح تشخيصًا دقيقًا وإجراءات وقائية موجّهة.
| Parameter | Our NGS Test | Sanger Sequencing (Alternative) |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity | ~99% detection rate |
| Methodology | Next‑Generation Sequencing (full gene) | Targeted exon Sanger sequencing |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Price (AED) | 2,800 | ~2,000 (limited analysis) |
Physician Insight & Safety Protocol
“As a physician caring for families affected by unexplained recurrent pyogenic infections, I find this test profoundly illuminating. A definitive genetic diagnosis of MYD88 deficiency allows us to move from empirical antibiotic cycles to targeted prophylaxis and immunoglobulin replacement, dramatically improving quality of life. However, I must stress that genetic results must always be correlated with clinical phenotype and immunological work‑up before finalising management.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Critical Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Altering prophylactic antibiotics or immune‑modulating therapy on your own can trigger life‑threatening infections.
🛑 Patient Exclusion Criteria
- Active unstable infection requiring hospitalisation.
- Inability to provide informed consent.
- Children under 2 years without prior paediatric genetic counselling.
🚨 Emergency Red Flags – Go to ER Immediately
- Fever >38.5°C with chills, hypotension, or confusion.
- Rapidly spreading skin abscess or cellulitis with systemic signs.
- Difficulty breathing or bluish lips.
These signs suggest sepsis or severe infection. Do not wait for sample collection; seek emergency care.
Patient FAQ & Clinical Guidance
What is MYD88 deficiency and how does the NGS test detect it?
MYD88 deficiency is a rare inherited disorder impairing immune defence against pyogenic bacteria and causing recurrent infections. The NGS test examines all coding exons of the MYD88 gene to identify pathogenic mutations, distinguishing this defect from other immunodeficiencies with similar clinical features. It is the most comprehensive method to confirm autosomal recessive MYD88 deficiency.
نقص MYD88 هو اضطراب وراثي نادر يضعف الاستجابة المناعية ضد البكتيريا القيحية مما يؤدي إلى عدوى متكررة. يكشف فحص التسلسل الجيني جميع الطفرات المسببة في الجين MYD88 لتأكيد التشخيص بدقة.
How do I prepare for the MYD88 genetic test?
Pre- preparation requires a clinical history review and genetic counselling session to document family pedigree for accurate variant interpretation. No fasting is needed. Provide a blood sample (whole blood, extracted DNA, or a dried blood spot on an FTA card) – our home collection team handles everything painlessly.
يتطلب التحضير جلسة استشارة وراثية لتوثيق شجرة العائلة وتاريخ المريض دون الحاجة للصيام. يتم جمع العينة منزليًا بكل سهولة.
What does a negative result mean for my child’s recurrent infections?
A negative result means no pathogenic MYD88 variant was detected, but other immunodeficiencies may still cause recurrent infections. Further immunological investigations (e.g., IgG subclass levels, complement studies) are recommended. Genetic counselling can help interpret the result in the family context.
النتيجة السلبية تعني عدم وجود طفرة في جين MYD88، لكن قد توجد اضطرابات مناعية أخرى. يُنصح بإجراء فحوصات مناعية إضافية واستشارة الوراثة.
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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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