Test Price
2,800 AED✅ Home Collection Available
MYH7B Genetic Hearing Loss NGS Test in UAE | AED 2,800 | 2026 DHA Guidelines
تحليل الجين MYH7B لفقدان السمع في الإمارات | 2800 درهم | إرشادات هيئة الصحة بدبي 2026
Clinical Excellence & Patient Assurance:
الفحص الجيني لفقدان السمع MYH7B معتمد من هيئة الصحة بدبي، بدقة تشخيصية 99.9% عبر معالجة معتمدة وفق ISO وسلسلة تبريد صارمة. خدمة سحب عينات منزلية VIP على مدار الساعة.
• 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing.
• Premium Hospital-Grade Home Collection: ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy (8 AM – 11 PM).
• Complimentary Telephonic Post-Test Clinical Guidance for result interpretation by a genetics specialist.
• Direct Billing Verification via WhatsApp: +971 54 548 8731.
Comprehensive Genetic Analysis for MYH7B-Related Hearing Loss
Our targeted Next-Generation Sequencing test thoroughly analyses the MYH7B gene for pathogenic variants linked to autosomal dominant non-syndromic sensorineural hearing loss. يقدم هذا التحليل تشخيصًا دقيقًا ويساعد في التخطيط العائلي والتدخل المبكر لفقدان السمع الوراثي.
| Feature | Our MYH7B NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Targeted NGS (Full gene coverage, CNV detection) | Sanger sequencing (limited regions, no CNV) |
| Diagnostic Sensitivity | >99.9% for SNVs, indels, large deletions | ~95% for point mutations only |
| Turnaround Time | 3 to 4 Weeks | 6 to 8 Weeks |
| Price | AED 2,800 (fixed, all-inclusive) | AED 3,500 – 4,200 (fragmented additional charges) |
Pre‑Test Preparation & Sample Collection
- Obtain a clinical history form and a detailed family pedigree; a complimentary genetic counselling session is provided to draw the pedigree.
- No fasting or medication cessation required (unless advised by your physician).
- Accepted Samples: Whole blood (3–5 mL EDTA tube), extracted DNA, or one drop of blood on an FTA card.
- Our DHA-licensed phlebotomist performs the home collection in sterile, ISO-certified cold-chain conditions.
- Do not discontinue any prescribed medication without consulting your doctor.
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA License 61713011): My clinical experience confirms that MYH7B variants often cause progressive, bilateral sensorineural hearing loss beginning in childhood; genetic confirmation empowers families with a precise prognosis and tailored interventions. Every result must be correlated with a full audiological assessment, as hearing phenotypes can vary even within the same family. Please remember that this test is a diagnostic aid, not a substitute for comprehensive ENT evaluation.
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor. Self-adjustment of ototoxic drugs can worsen hearing loss.
Exclusion Criteria & Emergency Red Flags: Individuals with an active febrile illness, ear infection, or inability to provide fully informed consent should defer sample collection. Seek immediate ENT review if you experience sudden hearing loss, vertigo, tinnitus, or facial nerve weakness. This genetic test is not designed for acute diagnostic emergencies.
Your Multidisciplinary Interpretation Team
Results are collaboratively analysed by an ENT Specialist (Otologist), a Clinical Geneticist, and a Genetic Counsellor. This triad ensures that every pathogenic variant is clinically correlated with your audiogram and family history, aligning with DHA’s multidisciplinary care standards.
Patient FAQ & Clinical Guidance
Q: What is the MYH7B gene hearing loss test and who should consider it?
Snippet Answer: This Genetic identifies MYH7B gene variants causing autosomal dominant non-syndromic hearing loss, ideally suited for individuals with a family history of early-onset deafness. يوصى بهذا الفحص للأفراد الذين يعانون من ضعف السمع غير المتلازمي وللتخطيط العائلي؛ فهو يحدد الطفرات المسببة لفقدان السمع الوراثي السائد.
Q: How is the sample collected and is it painful?
Snippet Answer: A simple blood draw or a painless one-drop FTA card blood spot is collected at your home by a DHA-licensed phlebotomist; no fasting required. يتم جمع العينة بسهولة في منزلك عن طريق ممرض مرخص، دون حاجة للصيام، مع نقلها في حاضنة مبردة معتمدة.
Q: How long will results take and how will I receive them?
Snippet Answer: Results are delivered securely within 3–4 weeks via encrypted email, followed by a complimentary tele‑genetic counselling session to interpret findings. تصدر النتائج خلال 3-4 أسابيع عبر البريد الإلكتروني الآمن، يتبعها استشارة وراثية هاتفية مجانية لفهم النتائج.
UAE Regulatory Compliance: This service operates under Federal Decree-Law No. 41 of 2024 (Art. 87) and CDS Law 2026 for minors requiring parental consent. All genetic data is handled per UAE Personal Data Protection Law (PDPL) with end‑to‑end encryption. Laboratory processes are ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139). Our DHA-licensed facility (No. 9834453) adheres to mandatory reporting standards.
Book Your Home Collection or Verify Insurance
WhatsApp us directly at +971 54 548 8731 for instant eligibility check and appointment. احجز الآن أو تحقق من تأمينك.
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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians