Test Price
1,800 AED✅ Home Collection Available
Myotonic Dystrophy Comprehensive Profile Test in UAE | 1800 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy: 99.9% diagnostic sensitivity via ISO 9001:2015 certified processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP mobile phlebotomy and temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic post-test guidance session included – interpreted by a Consultant Medical Geneticist.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
- Turnaround: Report by Friday if sample arrives by Monday 11 AM (5 working days).
Test Overview & Methodology
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 with a rapid 5‑day turnaround.
| Feature | Our Test (DNA Labs UAE) | 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 Protocols
“As a Consultant Medical Geneticist, I understand the anxiety that accompanies a potential diagnosis of myotonic dystrophy. This comprehensive profile provides the molecular clarity needed for early intervention and informed family planning. However, every result must be interpreted alongside a thorough clinical examination and genetic counselling. Our team is here to support you with empathy and expert guidance at every step.”
— Lina Osama Zaki Quteineh (Consultant Medical Genetics, DHA Registration ID: 9294403)
Advisory: Medication & Clinical Management
Do not discontinue any prescribed medication without consulting your doctor. Genetic results are not a substitute for ongoing clinical management. Always discuss findings with your referring physician.
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 Federal Decree-Law No. 4 of 2016 on Medical Liability 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
1. What exactly does the Myotonic Dystrophy Comprehensive Profile measure?
This genetic test detects CTG and CCTG repeat expansions in the 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.
2. Is the blood draw painful, and can I do it at home?
The sample collection is a standard peripheral venipuncture – a brief, minimally uncomfortable procedure comparable to a routine blood test. We offer VIP mobile phlebotomy and temperature-controlled cold-chain home collection 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.
3. How quickly will I receive my report, and who will explain it?
Your molecular report is released by Friday if the sample reaches our lab by Monday 11 am. A dedicated Consultant Medical Geneticist (Lina Osama Zaki Quteineh) 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.
UAE Regulatory & Data Privacy Adherence
UAE Healthcare Compliance: This service adheres to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All genetic data is stored securely within the UAE for 25 years as per DHA mandates. Clinical testing safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.
Accreditation: ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139). Genetic testing performed under DHA facility license 1143 at DNA Labs UAE.
For urgent inquiries or home collection booking, contact us 24/7 on +971 54 548 8731 (WhatsApp).
Clinical & Logistical Metadata
| Test Name | Myotonic Dystrophy Comprehensive Profile |
| Price (AED) | 1,800 |
| Turnaround Time | 5 working days (report by Friday if sample arrives Monday 11 AM) |
| Sample Type / Matrix | Whole blood (4 mL) – VIP mobile phlebotomy and temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM |
| Methodology Used | Triplet‑primed PCR + capillary electrophoresis + fragment/STR analysis |
| ICD-10-CM Code | G71.1 (Myotonic muscular dystrophy) |
| LOINC Code | 95113-4 (Myotonic dystrophy type 1 and type 2 comprehensive) |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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