Test Price
2,800 AED✅ Home Collection Available
RDX Gene Deafness (Autosomal Recessive Type 24) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين RDX للصمم الوراثي المتنحي النوع 24 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – ملخص تنفيذي
يوفر هذا الاختبار الجيني فحصًا دقيقًا لطفرات جين RDX المرتبطة بالصمم الوراثي المتنحي النوع 24، بنسبة حساسية تشخيصية تبلغ 99.9% ومطابقة لمعايير هيئة الصحة بدبي 2026. يتم إجراؤه في مختبراتنا الحاصلة على شهادة ISO 9001:2015.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy.
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Clinical Overview & Diagnostic Precision
The RDX Gene NGS Test screens for pathogenic variants in the RDX gene associated with autosomal recessive non-syndromic hearing loss type 24 (DFNB24). This comprehensive next-generation sequencing assay analyzes the entire coding region with high coverage, delivering diagnosis clarity for families. In the UAE, our DHA-licensed facility ensures result accuracy and genetic counselling support.
| Feature | Our NGS Test | Closest Alternative |
|---|---|---|
| Methodology | Next-Generation Sequencing (NGS) with full gene coverage & bioinformatics | Sanger sequencing of selected RDX exons; may miss deep intronic variants |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Detection Rate | >99% for point mutations, small indels, and splice site variants | Variable; limited to targeted regions |
| Cost | 2800 AED (all-inclusive) | Quoted separately; often excludes counselling |
Physician Insight & Safety Protocol
Clinical Note from Dr. PRABHAKAR REDDY (DHA: 61713011)
"As a clinical geneticist, I understand that hearing loss can be deeply concerning for families. This test is a powerful tool to uncover the genetic cause, but results must be correlated with detailed audiometric and clinical findings. Please remember, a negative result does not rule out other genetic or non-genetic causes; always consult your specialist."
⚠️ Important Safety & Medication Warning
Do not discontinue prescribed medications without consulting your doctor.
- Exclusion Criteria: None for the genetic test itself; however, inform the phlebotomist if you have a bleeding disorder or are on high-dose anticoagulants. An alternative specimen type (FTA card) may be recommended.
- ER Red Flags: Genetic testing for deafness does not carry immediate medical risks. If you experience sudden hearing loss or acute dizziness, seek emergency care independently of this test.
- Paediatric Use (CDS Law 2026): For minors, testing requires consent from a legal guardian and a referral from a DHA-licensed paediatric specialist. All paediatric data handling complies with UAE PDPL and Federal Decree-Law No. 41 of 2024 (Art. 87).
Patient FAQ & Clinical Guidance
1. What is the purpose of the RDX gene deafness NGS test?
ما الهدف من اختبار تسلسل جين RDX للصمم الوراثي؟
This sequences the RDX gene to identify mutations causing autosomal recessive deafness type 24, enabling precise genetic diagnosis and informed family planning.
يقوم هذا الاختبار بتسلسل جين RDX لتحديد الطفرات المسببة للصمم الوراثي المتنحي النوع 24، مما يتيح تشخيصًا جينيًا دقيقًا وتخطيطًا عائليًا مستنيرًا.
2. How is the sample collected and what is the preparation?
كيف يتم جمع العينة وما هو التحضير المطلوب؟
A blood sample or DNA sample is collected at home by our DHA-licensed phlebotomist; no fasting is required, but inform us of any medications.
يتم جمع عينة دم أو عينة حمض نووي في المنزل بواسطة فني سحب دم مرخص من هيئة الصحة بدبي؛ لا يشترط الصيام، لكن يُرجى إبلاغنا بأي أدوية تتناولها.
3. How long does it take to receive results and what does the report include?
كم من الوقت يستغرق استلام النتائج وماذا يتضمن التقرير؟
Results are delivered in 3 to 4 weeks with a comprehensive clinical report including variant interpretation and genetic counselling recommendations.
يتم تسليم النتائج خلال 3 إلى 4 أسابيع مع تقرير سريري شامل يتضمن تفسير المتغيرات وتوصيات الاستشارة الوراثية.
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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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