CD36 Gene (Platelet Glycoprotein IV Deficiency) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل CD36 Gene Platelet Glycoprotein IV Deficiency Genetic Test في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

🔬 Accuracy | 🚚 Logistics | 🩺 Clinical Guidance

Diagnostic Sensitivity 99.9% – ISO 9001:2015 accredited processing using NGS technology.
Hospital‑Grade Home Collection – ISO‑certified cold‑chain transportation and VIP mobile phlebotomy (8 AM–11 PM).
Telephonic Post‑Test Guidance – Expert clinical interpretation by a DHA‑licensed hematologist.
Direct Insurance Billing Verification – Contact via +971 54 548 8731 (WhatsApp available).

الملخص التنفيذي بالعربية

فحص الجين CD36 (نقص البروتين السكري الرابع) عبر تقنية التسلسل الجيني من الجيل التالي (NGS) في مختبر معتمد دوليًا وفق معايير ISO 9001:2015 وشهادة هيئة الصحة بدبي، يضمن دقة تشخيصية بنسبة 99.9% مع استشارة وراثية متكاملة وحماية بيانات المرضى وفق قانون الإمارات لحماية البيانات الشخصية (PDPL) والقانون الاتحادي رقم 41 لسنة 2024 المادة 87، إضافةً إلى توجيهات قانون حماية بيانات الطفل 2026 للقُصّر.

Quick Overview

The CD36 Gene NGS Test screens for pathogenic variants causing platelet glycoprotein IV deficiency, a hereditary bleeding disorder. يفحص هذا التحليل الطفرات الجينية في جين CD36 المسؤولة عن نقص البروتين السكري الرابع ويُستخدم للتشخيص والاستشارة الوراثية العائلية.

Feature	Our CD36 NGS Test	Closest Alternative
Precision	99.9% sensitivity; coverage of entire coding region & splice sites	Sanger sequencing – limited to known hotspots
Method	Next‑Generation Sequencing (NGS) – multi‑gene analysis possible	Single‑gene PCR + capillary electrophoresis
Turnaround Time	3–4 Weeks	4–6 Weeks (depending on lab)
Genetic Counseling	Mandatory pre‑test session with pedigree mapping (included)	Often not integrated; additional referrals needed

Physician Insight & Safety Protocol

“As a hematologist, I understand the emotional weight of pursuing a genetic diagnosis for a bleeding disorder. This test provides definitive molecular confirmation, but it must always be correlated with your personal and family clinical story. My team and I are dedicated to delivering compassionate, evidence‑based guidance every step of the way.”

— Dr. Prabhakar Reddy, DHA License No. 61713011

⚠ Important Medication Warning

Do not discontinue any prescribed medication, especially antiplatelets or anticoagulants, without explicit consultation with your treating physician. This genetic test does not provide immediate therapeutic guidance.

Safety Exclusion Criteria & Emergency Red Flags

Specimen collection is not performed on individuals with active, untreated bleeding diathesis unless cleared by a physician.
Patients on high‑dose anticoagulants must disclose their regimen; home phlebotomy may still proceed with caution.
Genetic testing of minors requires parental consent as per UAE Child Data Safeguard (CDS) Law 2026.
ER Red Flags: If you experience prolonged bleeding (>15 min), large hematoma, dizziness, or signs of infection at the draw site after blood collection, seek immediate medical attention.

Patient FAQ & Clinical Guidance

What is the CD36 gene test and why is it performed?

This NGS‑based test analyzes the entire CD36 gene to detect mutations causing glycoprotein IV deficiency, a bleeding disorder. It is ordered when a patient presents with unexplained mucocutaneous bleeding, thrombocytopenia, or a family history suggestive of a platelet disorder. The result helps confirm the diagnosis, guide management, and inform genetic counseling for at‑risk relatives.

How should patients prepare for the CD36 genetic test?

A pre‑ genetic counseling session and pedigree charting are mandatory to ensure accurate interpretation and informed consent. During this visit, the clinician reviews your bleeding history, medication list, and constructs a family tree. The sample itself requires no fasting; a small amount of blood (EDTA tube) or a dried blood spot on an FTA card is collected by a certified phlebotomist.

هل جمع عينة الدم لإجراء تحليل CD36 مؤلم للأطفال؟

يتم جمع العينة عن طريق وخز الإصبع أو الوريد بطريقة متخصصة تخفف الألم بشكل كبير تحت إشراف فني معتمد. يُستخدم كريم تخدير موضعي لتقليل الإحساس، وتُفضل بطاقة FTA للأطفال لأنها تحتاج قطرة دم واحدة فقط. يُشترط حضور الوالدين وتوقيع الموافقة وفقًا لقانون حماية بيانات الطفل الإماراتي لعام 2026.

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