Test Price
2,800 AEDโ Home Collection Available
FKTN Gene Limb-Girdle Muscular Dystrophy Autosomal Recessive Type 2M (LGMDR2M) Genetic Test in UAE
Executive Summary & Core Metrics
This comprehensive genetic test utilizes Next-Generation Sequencing (NGS) to detect pathogenic variants in the FKTN gene associated with autosomal recessive limb-girdle muscular dystrophy type 2M (LGMDR2M). With 99.9% diagnostic sensitivity, it is performed at our ISO 9001:2015 certified laboratory under DHA License 1143. The test includes VIP mobile phlebotomy and temperature-controlled cold-chain home collection, with results delivered within 3โ4 weeks.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (available daily 8 AM โ 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
- Price: 2,800 AED.
Test Overview & Methodology
The FKTN gene NGS test analyzes the entire coding region of the FKTN gene to detect pathogenic variants responsible for limb-girdle muscular dystrophy autosomal recessive type 2M (LGMDR2M). Our facility offers the most comprehensive sequencing with ISO 9001:2015 accreditation and a rapid 3โ4 week turnaround.
| Feature | Our Test (NGS Full Gene Sequencing) | Common Alternative (Single Exon / Panel) |
|---|---|---|
| Precision | 99.9% diagnostic sensitivity | May miss deep intronic variants |
| Method | Next Generation Sequencing (Illumina NovaSeq) | Sanger sequencing limited regions |
| Speed | 3โ4 Weeks | Varies, often 6+ weeks |
Physician Insight & Safety Protocols
"As a Consultant Medical Genetics, I emphasize that identifying a pathogenic FKTN variant provides a genetic diagnosis that must be integrated with a detailed clinical evaluation and family history. Genetic testing is a powerful tool for confirming limb-girdle muscular dystrophy type 2M and guiding management, including cardiac and respiratory surveillance. It is essential to interpret results in the context of the patient's overall condition and never to change treatments based solely on genetic data." โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory on Medication Management
Do not discontinue or adjust any prescribed medication without consulting your treating physician. Genetic test results do not replace professional medical advice regarding drug therapy.
Exclusion Criteria & Safety Precautions
- Not suitable for patients with acute severe illness requiring urgent care; defer testing until stable.
- If you experience sudden muscle weakness, breathing difficulties, or cardiac symptoms, immediately visit the emergency departmentโdo not wait for test results.
- Minors (under 18) must be accompanied by a legal guardian with valid consent as per UAE Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Home collection is excluded if the patient cannot provide a safe phlebotomy environment or has a known significant bleeding disorder.
ER Red Flags: Acute respiratory distress, severe dysphagia, loss of ambulation within days, chest pain.
Patient FAQ & Clinical Guidance
1. What does the FKTN gene test detect and how can it help my family?
This test identifies pathogenic variants in the FKTN gene responsible for autosomal recessive limb-girdle muscular dystrophy type 2M, enabling accurate diagnosis, carrier screening, and informed family planning. By sequencing the entire coding region via NGS, we detect even rare mutations that single-gene panels might miss. This information helps your neurologist tailor rehabilitation, monitor cardiac involvement, and assess eligibility for emerging gene therapies.
2. How is the sample collected and is it painful?
A simple blood draw into an EDTA tube or a painless buccal swab is used. Our certified phlebotomist performs VIP home collection. The sample is transported in a temperature-monitored cold-chain to our Dubai laboratory. Results are ready in 3โ4 weeks.
3. Is my genetic data confidential and protected under UAE law?
Absolutely. Your genetic information is safeguarded under 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 data is encrypted and stored on secure servers accessible only to authorized physicians. We never share identifiable data without your explicit consent.
UAE Regulatory & Data Privacy Adherence
Our laboratory strictly adheres to the UAE's data protection and health information regulations, including 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 encrypted, stored securely, and accessible only to authorized personnel. Patient consent is obtained in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability. We are committed to maintaining the highest standards of privacy and security.
Clinical & Logistical Metadata
| Test Name | FKTN Gene Limb-Girdle Muscular Dystrophy Autosomal Recessive Type 2M (LGMDR2M) Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA) or Buccal Swab |
| Methodology Used | Next-Generation Sequencing (NGS) โ Full Gene Sequencing |
| ICD-10-CM Code | G71.0 |
| LOINC Code | 82939-0 |
| DHA Facility License & Address | License: 1143 โ Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians