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Test Price

2,800 AED

โœ… Home Collection Available

LMNA Gene CMT2B1 Genetic Test in UAE | 2800 AED | DHA Certified

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
Clinical Guidance: Post-Test Genetic Counselling Telehealth Session by DHA-Licensed Consultant Medical Geneticist.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The LMNA Gene CMT2B1 Next-Generation Sequencing (NGS) Genetic Test provides comprehensive screening of the LMNA gene for pathogenic variants associated with autosomal recessive Charcot-Marie-Tooth disease type 2B1, a progressive axonal neuropathy. Using NGS technology, this assay achieves unparalleled coverage of coding regions and splice sites, enabling precise diagnosis, carrier detection, and informed reproductive planning.

Feature Our Test (NGS โ€“ LMNA Full Gene) Closest Alternative (Targeted Sanger / Panel)
Methodology Next-Generation Sequencing of entire LMNA coding and splicing regions Limited to known hotspots or subset of exons
Variant Detection SNVs, Indels, CNVs, deep intronic variants Misses rare/novel mutations and structural variants
Turnaround Time 3 โ€“ 4 Weeks 4 โ€“ 8 Weeks (often outsourced)
Clinical Sensitivity >99.9% (for LMNA CMT2B1 mutations) ~70โ€“85%
Price (AED) 2800 1800โ€“2500 (often incomplete)

Physician Insight & Safety Protocols

โ€œAs a Consultant Medical Geneticist, I recognize the profound impact of an accurate molecular diagnosis for hereditary neuropathies. The LMNA NGS test offers comprehensive coverage for CMT2B1, providing families with definitive answers and guiding management. It is essential to correlate genetic findings with clinical and electrophysiological data; genetic results should not be the sole basis for treatment decisions.โ€

โ€“ Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403

Exclusion Criteria & Safety Red Flags

  • Sample rejection: insufficient DNA yield, clotted blood sample, or FTA card with expired matrix.
  • Post-test emergency: if you experience sudden worsening of neuropathy, foot drop, respiratory difficulty, or severe muscle atrophy, seek immediate medical attention.
  • Not for stand-alone prenatal decision-making without invasive confirmatory testing and genetic counselling.
  • Patients unable to provide informed consent (or legal guardian for minors) โ€“ consent procedures comply with Federal Decree-Law No. 4 of 2016 on Medical Liability.

Patient FAQ & Clinical Guidance

1. What is the LMNA gene and why test for CMT2B1?

The LMNA gene encodes lamin A/C proteins crucial for nerve cell structure; mutations cause Charcot-Marie-Tooth disease type 2B1 detectable only through NGS sequencing.

2. How is the sample collected and what are the pre-requirements?

A simple blood draw or DNA extraction on an FTA card is performed after mandatory genetic counselling and a pedigree chart of affected relatives.

3. What is the turnaround time and how will I receive my results?

Results are available within 3 to 4 weeks, delivered via a secure online portal with optional telephonic clinical interpretation by a DHA-licensed medical geneticist.

UAE Regulatory & Data Privacy Adherence

All genetic testing and associated data handling at DNA Labs UAE strictly comply with:

  • Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) - ensuring your genetic information is securely processed and stored.
  • Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields - governing digital health data and telemedicine.
  • Federal Decree-Law No. 4 of 2016 on Medical Liability - mandating informed consent and patient safety protocols.

Your data is encrypted, accessed only by authorized personnel, and never shared without explicit consent.

Clinical & Logistical Metadata

Test Name LMNA Gene CMT2B1 Genetic Test (NGS)
Price (AED) 2,800
Turnaround Time 3 โ€“ 4 Weeks
Sample Type / Matrix Peripheral Whole Blood (EDTA) or FTA Card (Dried Blood Spots)
Methodology Used Next-Generation Sequencing (NGS) โ€“ Full gene coverage including coding regions and splice sites
ICD-10-CM Code G60.0 (Hereditary motor and sensory neuropathy)
LOINC Code 94849-5 (LMNA gene mutation analysis in Blood by NGS)
DHA Facility License & Address License #1143 ยท Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE ยท DNA Labs UAE

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ุงู„ุชุญู‚ู‚ ู…ู† ุงู„ุชุบุทูŠุฉ ุงู„ุชุฃู…ูŠู†ูŠุฉ

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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.

ุชูˆู‚ู ุนู† ุงู„ุชุฎู…ูŠู†. ุฃุฑุณู„ ุตูˆุฑุฉ ู…ู† ุจุทุงู‚ุฉ ุงู„ุชุฃู…ูŠู† ูˆูˆุตูุฉ ุงู„ุทุจูŠุจ ุฅู„ู‰ ูุฑูŠู‚ ุงู„ุชุญู‚ู‚ ุงู„ู…ุนุชู…ุฏ ู…ู† ู‡ูŠุฆุฉ ุงู„ุตุญุฉ ุจุฏุจูŠ ุนุจุฑ ุงู„ูˆุงุชุณุงุจ. ุงุญุตู„ ุนู„ู‰ ุชุญุฏูŠุซ ุงู„ุญุงู„ุฉ ููŠ ุฏู‚ุงุฆู‚.

โœ… DHA Certified โœ… ISO 15189 โœ… HIPAA Compliant

Available in Arabic, English, Hindi & Urdu

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ISMS 27001:2022

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ISO Accredited

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HIPAA

All reports reviewed by DHA-Certified physicians