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Test Price

2,800 AED

✅ Home Collection Available

RSPH4A Gene Primary Ciliary Dyskinesia Type 11 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين RSPH4A لخلل الحركة الهدبية الأولي النوع 11 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

Executive Summary | الملخص التنفيذي

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing.
  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation with DHA-licensed specialists.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

خدمة معتمدة من هيئة الصحة بدبي لعام 2026 تشمل استشارة وراثية متخصصة.

Test Overview / نظرة عامة

RSPH4A gene testing using Next-Generation Sequencing (NGS) comprehensively identifies pathogenic mutations responsible for primary ciliary dyskinesia type 11, a rare autosomal recessive disorder. This test, tailored for the UAE population, combines high-resolution sequencing with CNV detection to ensure diagnostic precision superior to single-gene methods.

Feature Our Test (NGS) Sanger Sequencing (Alternative)
MethodNext-Generation Sequencing (NGS)Sanger Sequencing
Turnaround Time3–4 Weeks4–6 Weeks
ComprehensivenessFull gene + CNV analysisLimited to specific exons
Price2800 AED~3500 AED

Sample accepted: Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card). Pre-test genetic counseling recommended.

Physician Insight & Safety Protocol

"As a DHA-licensed ENT specialist and clinical genetic testing expert (License 61713011), I reassure you that this test provides robust confirmation of primary ciliary dyskinesia type 11, enabling precise management and family planning. Results must always be integrated with clinical symptoms—chronic sinusitis, bronchiectasis, situs inversus—and discussed with a genetic counselor for actionable insights." – Dr. Prabhakar Reddy.

⚠️ Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & Emergency Red Flags

  • This test is not suitable for individuals lacking informed consent or those with unstable acute illness requiring immediate intervention.
  • Sample collection should be postponed if the patient exhibits severe, uncontrolled coagulopathy.
  • ER Red Flags:
  • If you experience sudden severe respiratory distress, high fever (>39°C), or acute chest pain, seek emergency care immediately—these are not direct complications of sample collection but require urgent attention.

Compliance: This test fully adheres to Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), UAE PDPL, and current DHA guidelines. ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139). Genetic testing of minors requires documented parental consent.

Patient FAQ & Clinical Guidance

What is the RSPH4A gene test used for?

This genetic test detects RSPH4A mutations confirming primary ciliary dyskinesia type 11, guiding targeted treatment and family screening.

ما هو تحليل جين RSPH4A؟

يكشف تحليل جين RSPH4A عن الطفرات المسببة لخلل الحركة الهدبية الأولي النوع 11، ويساعد في توجيه العلاج المناسب والفحص العائلي.

How is the sample collected and what is the turnaround time?

A certified phlebotomist collects blood, a dried spot, or extracted DNA at your home; results are ready in 3–4 weeks.

كيف يتم جمع العينة وما هي مدة الحصول على النتيجة؟

يقوم أخصائي سحب عينات مرخص بجمع عينة دم أو بقعة دم جافة من منزلك، وتصدر النتائج خلال 3 إلى 4 أسابيع.

Does insurance cover this genetic in UAE?

Most UAE insurers cover medically necessary genetic testing; verify your eligibility and direct billing via WhatsApp at +971 54 548 8731.

هل يشمل التأمين الصحي تحليل الجين RSPH4A في الإمارات؟

تغطي معظم شركات التأمين في الإمارات التحاليل الجينية الضرورية؛ تأكد من تغطيتك وخدمة الفوترة المباشرة عبر واتساب على الرقم 0545488731.

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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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