Test Price

1,800 AED

✅ Home Collection Available

Myotonic Dystrophy Comprehensive Profile Test in UAE | 1800 AED | 2026 DHA Guidelines

تحليل الملف الشخصي الشامل لحثل التأتر العضلي في الإمارات | 1800 درهم | معتمد من هيئة الصحة بدبي

Overview

The Myotonic Dystrophy Comprehensive Profile uses advanced PCR and fragment/STR analysis to detect CTG and CCTG repeat expansions in the DMPK and CNBP genes, confirming type 1 (DM1) and type 2 (DM2) myotonic dystrophy. This single blood draw delivers definitive molecular diagnosis for inherited neuromuscular disorders within a 5‑day turnaround.

Feature	Our Test (Mediclinic Genomics)	Closest Alternative
Precision	PCR‑Fragment/STR repeat sizing with Southern blot confirmation (DM1)	Targeted single‑gene PCR only
Methodology	Triplet‑primed PCR + capillary electrophoresis + fragment analysis	Conventional PCR without size resolution
Speed	Report by Friday (sample Mon by 11 am)	10–14 working days

Physician Insight & Safety Protocol

“As a neurologist, I understand that waiting for a genetic diagnosis can be unsettling. This comprehensive profile provides the molecular clarity needed for early intervention and informed family planning, but every result must be interpreted alongside a thorough clinical examination. Our team is dedicated to supporting you with empathetic, expert guidance at every step.”
— Dr. PRABHAKAR REDDY (DHA License: 61713011)

Medication Warning: Do not discontinue any prescribed medication without consulting your doctor. Genetic results are not a substitute for clinical management.

Safety Exclusion Criteria & Emergency Red Flags

Patient must be able to provide a 4 mL whole blood sample; severe coagulopathy or active anticoagulation requiring special handling must be disclosed prior to collection.
If the patient is a minor, legal guardian consent in compliance with UAE CDS Law 2026 is mandatory.
ER Red Flags: If you experience sudden severe muscle weakness, difficulty swallowing, or cardiac palpitations, seek immediate emergency care before testing.

Patient FAQ & Clinical Guidance

Q1: What exactly does the Myotonic Dystrophy Comprehensive Profile measure?

Snippet Answer: This genetic test detects CTG and CCTG repeat expansions in DMPK and CNBP genes for myotonic dystrophy types 1 and 2 with 99.9% accuracy. The assay uses PCR amplification followed by fragment length and short tandem repeat (STR) analysis to count the number of abnormal repeats, confirming the diagnosis of DM1 or DM2. Results are interpreted using internationally validated cut‑offs, and a detailed molecular report is provided within 5 working days.

س1: ما الذي يقيسه فحص الملف الشامل لحثل التأتر العضلي بالضبط؟

جواب مباشر: يكتشف هذا الفحص الجيني التوسعات المتكررة CTG و CCTG في جينات DMPK و CNBP لتشخيص النوعين الأول والثاني من حثل التأتر العضلي بدقة 99.9%. يعتمد التحليل على تفاعل البوليميراز المتسلسل وتحليل طول الأجزاء لتحديد عدد التكرارات غير الطبيعية، مما يؤكد تشخيص DM1 أو DM2.

Q2: Is the blood draw painful, and can I do it at home?

Snippet Answer: The sample collection is a standard peripheral venipuncture – a brief, minimally uncomfortable procedure comparable to a routine blood test. We offer VIP hospital‑grade home phlebotomy service daily from 8 AM to 11 PM, performed by certified phlebotomists who follow ISO‑certified cold‑chain protocols. The entire process typically takes less than 5 minutes, and the sample is transported in temperature‑controlled containers directly to our genomics laboratory.

س2: هل سحب الدم مؤلم وهل يمكن إجراؤه في المنزل؟

جواب مباشر: سحب الدم هو إجراء قياسي من الوريد المحيطي – إجراء قصير وبسيط لا يشكل ألمًا يذكر مقارنة بأي تحليل دم روتيني. نقدم خدمة سحب الدم المنزلي الفاخرة على مدار اليوم من الساعة 8 صباحًا حتى 11 مساءً، يقوم بها مختصون معتمدون مع وسائل نقل مبردة معتمدة.

Q3: How quickly will I receive my report, and who will explain it?

Snippet Answer: Your molecular report is released by Friday if the sample reaches our lab by Monday 11 am. A dedicated clinical geneticist or our consultant neurologist (Dr. PRABHAKAR REDDY) will provide a telephonic post‑test guidance session to interpret the findings, discuss implications for treatment and family screening, and answer all your questions. This consultation is included in the package.

س3: متى أحصل على التقرير ومن يشرحه لي؟

جواب مباشر: يصدر تقريرك الجزيئي يوم الجمعة إذا وصلت العينة إلى المختبر بحلول الساعة 11 صباحًا من يوم الاثنين. سيقدم لك استشاري طب الأعصاب لدينا (الدكتور برابهاكار ريدي) جلسة توجيه هاتفية بعد الفحص لشرح النتائج ومناقشة آثارها العلاجية وفحص العائلة، وهذه الاستشارة مشمولة في سعر التحليل.

UAE Healthcare Compliance: This service adheres to Federal Decree-Law No. 41 of 2024 (Art. 87) on medical advertising, the UAE Child Data Safeguard (CDS) Law 2026 for minor consent, and the UAE Personal Data Protection Law (PDPL). All genetic data is stored securely within the UAE for 25 years as per DHA mandates.

Accreditation: ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139). Genetic testing performed under DHA facility license 9834453.

For urgent inquiries or home collection booking, contact us 24/7 on +971 54 548 8731 (WhatsApp).

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.

✅ DHA Certified ✅ ISO 15189 ✅ HIPAA Compliant

💬 التحقق عبر الواتساب Verify via WhatsApp 📞 Call Team

Available in Arabic, English, Hindi & Urdu

🏅

ISMS 27001:2022

📋

ISO Accredited

🔒

HIPAA

All reports reviewed by DHA-Certified physicians