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Test Price

2,800 AED

✅ Home Collection Available

CD79A Gene Agammaglobulinemia Type 3, Autosomal Recessive Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين CD79A لمرض نقص غاما غلوبولين الدم من النوع الثالث المتنحي الجسدي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

Executive Summary:

99.9% Diagnostic Sensitivity via ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) Accredited Processing. Paid Hospital‑Grade Home Collection with Cold‑Chain Logistics and VIP Mobile Phlebotomy. Telephonic Post‑Test Clinical Guidance to interpret results. Direct Billing Verification via WhatsApp: +971 54 548 8731.

ملخص تنفيذي: يقدم هذا الفحص الجيني الدقيق لتشخيص طفرة جين CD79A المسؤولة عن نقص غاما غلوبولين الدم من النوع الثالث المتنحي الجسدي، مع خدمة سحب منزلي معتمدة وتوجيه استشاري هاتفي بعد النتيجة، وضمان دقة 99.9% وفق معايير الجودة ISO.

Test Overview

The CD79A Gene Agammaglobulinemia Type 3 Test uses next‑generation sequencing (NGS) to sequence the entire coding region of the CD79A gene, confirming autosomal recessive agammaglobulinemia – a life‑threatening primary immunodeficiency marked by absent B cells and profound hypogammaglobulinemia. يساعد الأطباء المختصين في أمراض الدم والمناعة على وضع خطة علاجية مبكرة تشمل بدائل الغلوبولين المناعي.

Feature Our Test (NGS) Closest Alternative (Sanger Sequencing)
Methodology Full‑Gene Next‑Generation Sequencing (Illumina‑based) Single‑variant or limited‑region Sanger sequencing
Detection Rate ≥99.9% sensitivity for known and novel CD79A variants ~85% – only known hotspots; novel variants missed
Turnaround Time 3‑4 Weeks 5‑7 Days (limited scope)

Physician Insight & Safety Protocol

Clinical Note from Dr. Prabhakar Reddy (DHA License: 61713011):
I know that confronting the possibility of a severe primary immunodeficiency in your child or a family member is deeply unsettling. This test provides definitive molecular evidence that eliminates diagnostic uncertainty, allowing us to initiate life‑saving immunoglobulin replacement and to offer precise genetic risk counselling for the entire family. However, the genetic result must be interpreted alongside immunophenotyping and clinical history – no single assay stands alone.

🔴 Do not discontinue prescribed medication without consulting your doctor.

🛡️ Safety & Exclusion Criteria

  • Test is intended for individuals with clinical suspicion of agammaglobulinemia (recurrent severe infections, absent B‑cells). Family screening should follow genetic counseling.
  • If the patient develops high fever, severe respiratory distress, or signs of sepsis before the scheduled blood draw, proceed to the nearest Emergency Department immediately. Do not delay urgent care to obtain the sample.

Patient Frequently Asked Questions & Clinical Guidance

What does the CD79A gene test detect?

This identifies all pathogenic and likely pathogenic variants in the CD79A gene with 99.9% diagnostic sensitivity, confirming the molecular cause of autosomal recessive agammaglobulinemia type 3.

يكشف هذا التحليل جميع الطفرات الممرضة في جين CD79A بدقة 99.9% لتأكيد تشخيص نقص غاما غلوبولين الدم المتنحي الجسدي.

How is the sample collected and prepared?

We offer 8 AM – 11 PM hospital‑grade home collection by a DHA‑licensed phlebotomist; a single 2 mL EDTA whole blood or one‑drop blood on FTA card is sufficient, with no fasting required.

نوفر خدمة سحب منزلي معتمدة من هيئة الصحة بدبي بين 8 صباحاً و11 مساءً، وعينة دم كامل في أنبوب EDTA واحدة تكفي.

What is the turnaround time and how are results delivered?

Results are reported within 3 to 4 weeks through a secure, DHA‑compliant portal, and include a tele‑genetic counselling session to interpret findings and plan family screening.

تظهر النتائج خلال 3 إلى 4 أسابيع عبر بوابة آمنة معتمدة، مع جلسة استشارة هاتفية متخصصة لتفسيرها.

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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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