Test Price
2,800 AED✅ Home Collection Available
ARHGEF10 Gene Slowed Nerve Conduction Velocity, Autosomal Dominant Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين ARHGEF10 لتباطؤ سرعة التوصيل العصبي، الوراثي السائد بتقنية NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- 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 (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation with DHA-certified experts.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
نقدم تحليل جين ARHGEF10 بدقة تشخيصية تصل إلى 99.9% عبر مختبر معتمد وفق ISO 9001:2015، مع خدمة جمع العينات المنزلية المبردة، وإرشاد طبي بعد النتائج، والتحقق من التغطية التأمينية عبر واتساب. الامتثال الكامل للمرسوم بقانون اتحادي رقم 41 لسنة 2024 وقانون حماية البيانات الشخصية الإماراتي يضمن خصوصية معلوماتك الجينية.
Clinical Overview
This advanced genetic test utilizes Next-Generation Sequencing (NGS) to analyze the entire coding region of the ARHGEF10 gene, identifying single nucleotide variants, small insertions/deletions, and copy number variations responsible for autosomal dominant slowed nerve conduction velocity, a hereditary neuropathy. يُحلل الاختبار جين ARHGEF10 بدقة فائقة لتشخيص الاعتلال العصبي الوراثي السائد المرتبط بتباطؤ سرعة التوصيل العصبي.
| Feature | Our Test (Gold Standard) | Closest Alternative |
|---|---|---|
| Precision | 99.9% sensitivity via NGS | Sanger sequencing (85% sensitivity, single gene) |
| Method | NGS (Illumina NovaSeq X Plus) with CNV calling | Capillary electrophoresis Sanger |
| Turnaround Time | 3 to 4 weeks | 6 to 8 weeks |
Physician Insight & Safety Protocol
“As a DHA-licensed neurologist, I emphasize that the ARHGEF10 genetic test is a powerful diagnostic tool, but it must be interpreted alongside a comprehensive clinical evaluation, nerve conduction studies, and family history. A positive result confirms the molecular etiology, while a negative result does not exclude other hereditary neuropathies. Please maintain all current treatments and consult your doctor before making any changes.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011, Consultant Neurologist
⚠️ Medication & Safety Warning
Do not discontinue any prescribed medication without consulting your treating physician. This genetic test is not a replacement for acute neurological assessment.
Exclusion Criteria & Emergency Red Flags
- Inability to provide informed consent or lack of legal guardian consent (mandatory for minors per CDS Law 2026).
- Sample collected in non-DNA-stabilizing tube, insufficient volume, or severe hemolysis.
- Acute neurological symptoms such as sudden bilateral weakness, vision loss, slurred speech, or seizure require immediate emergency care—do not wait for this test.
Frequently Asked Questions
What is the ARHGEF10 gene test?
This NGS test identifies ARHGEF10 gene variants responsible for autosomal dominant slowed nerve conduction velocity neuropathy.
It examines the DNA sequence of the ARHGEF10 gene to detect pathogenic mutations causing hereditary neuropathy with slowed nerve conduction speeds. It aids in accurate diagnosis, family risk assessment, and informed management.
يكشف هذا الاختبار طفرات جين ARHGEF10 الموروثة السائدة المسؤولة عن اعتلال الأعصاب الوراثي. يُستخدم لتأكيد التشخيص السريري وتوجيه الاستشارة الوراثية العائلية.
How is the specimen collected?
A simple blood draw or a drop of blood on an FTA card is collected by a certified phlebotomist during our home visit.
Samples can be whole blood (5 mL in EDTA tube), extracted DNA, or a dried blood spot on an FTA card. Our VIP mobile phlebotomy team follows strict cold-chain protocols to preserve DNA integrity, available daily from 8 AM to 11 PM.
يتم جمع العينة عبر سحب دم وريدي بسيط أو نقطة دم على بطاقة FTA بواسطة أخصائي معتمد خلال الزيارة المنزلية. نضمن نقل العينة مبردة وفق المعايير الدولية.
Is pre-test genetic counselling required?
Yes, a mandatory genetic counselling session and pedigree chart documentation are required before sample collection per DHA 2026 guidelines.
This ensures informed consent, a detailed three-generation family history, and appropriate selection. Our team arranges a telehealth counselling session at your convenience.
نعم، جلسة الاستشارة الوراثية وتخطيط شجرة العائلة إلزامية قبل سحب العينة وفق توجيهات هيئة الصحة بدبي. نقدم الاستشارة عن بُعد مع خبراء الوراثة.
Laboratory Accreditation: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Facility Licensed by DHA/MOHAP: 9834453.
Legal Compliance: This service adheres to UAE Federal Decree-Law No. 41 of 2024 (Art. 87), the 2026 CDS Law (Minors) concerning genetic testing in minors, and the UAE Personal Data Protection Law (PDPL). All genetic data is processed locally.
Contact & Home Collection: +971 54 548 8731 / WhatsApp here. Service hours 8:00 AM – 11:00 PM, 7 days a week.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
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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All reports reviewed by DHA-Certified physicians