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Genetics

Neuromuscular Genetics Tests in Dubai & UAE

Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.

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  • Home collection across the UAE
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Neuromuscular Genetics investigations

All 15 investigations in this category are listed below.

Neuromuscular Genetics tests offered by DNA Labs UAE — compare specimen type, turnaround time and listed price. Preparation and clinical interpretation are confirmed with your clinician before collection.
Test What it measures Specimen Turnaround Price Book
ACTA1 Gene Myopathy with Fiber‑Type Disproportion Genetic Test TEST-5238 LOINC 78603-1 This genetic test analyzes the ACTA1 gene for mutations associated with congenital myopathy with fibre-type disproportion. Whole Blood (Peripheral) 3–4 Weeks 2,800.00 AED Details
B3GALNT2 Gene NGS Test for Congenital Muscular Dystrophy with α‑Dystroglycan Hypoglycosylation TEST-4140 LOINC 62357-4 This test evaluates the B3GALNT2 gene for pathogenic variants associated with congenital muscular dystrophy-dystroglycanopathy. Peripheral Whole Blood, Extracted DNA, or FTA Card 3 – 4 Weeks 2,800.00 AED Details
BIN1 Gene Centronuclear Myopathy Type 2 Genetic Test TEST-3955 LOINC 81315-1 This genetic test analyzes the BIN1 gene for mutations associated with Centronuclear Myopathy Type 2. Whole blood (EDTA), FTA card, or extracted DNA 3–4 weeks 2,800.00 AED Details
CHRNE Gene Congenital Myasthenic Syndrome Genetic Test TEST-5296 LOINC 82318-0 This genetic test identifies mutations in the CHRNE gene, a common cause of congenital myasthenic syndrome (CMS). It helps establish a definitive diag... Whole blood (EDTA) or buccal swab 3–4 weeks 2,800.00 AED Details
CRYAB Gene (Desmin-Related Myopathy) Genetic Test TEST-5246 LOINC 82104-7 This genetic test identifies pathogenic variants in the CRYAB gene associated with desmin-related myofibrillar myopathy. Whole Blood (EDTA), Extracted DNA (≥1 µg at ≥50 ng/µL), or FTA Card Blood Spot 21–28 Days 2,800.00 AED Details
DES Gene Myofibrillar Myopathy (Desmin‑Related) Genetic Test TEST-5358 LOINC 101031-5 This genetic test identifies mutations and copy number variations within the DES gene, which are causative for desmin-related myofibrillar myopathy. Whole blood (EDTA tube, 2–5 mL), Extracted DNA (≥1 µg, concentration ≥25 ng/µL), or Dried Blood Spot on FTA Card (≥3 circles) 3–4 weeks from receipt of properly collected sample and completed pedigree 2,800.00 AED Details
DNAJB6 Gene Limb-Girdle Muscular Dystrophy, Autosomal Dominant Type 1E (LGMD1E) Genetic Test TEST-4714 LOINC 85726-1 This test evaluates the DNAJB6 gene for pathogenic variants associated with Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1E (LGMD1E). Whole blood (EDTA tube) or dried blood spot (FTA card) 3–4 Weeks 2,800.00 AED Details
GNE Gene Nonaka Myopathy Genetic Test TEST-5390 LOINC 21636-6 This test screens the entire GNE gene coding region for pathogenic variants associated with Nonaka myopathy. Peripheral whole blood (EDTA tube) 3–4 weeks 2,800.00 AED Details
LMNA Gene Limb‑Girdle Muscular Dystrophy Type 1B (LGMD1B) Genetic Test TEST-4711 LOINC 88215-1 This genetic test analyzes the LMNA gene to detect mutations associated with Limb-Girdle Muscular Dystrophy Type 1B (LGMD1B). It identifies pathogenic... Peripheral whole blood (3 mL EDTA tube) 3–4 Weeks 2,800.00 AED Details
MEGF10 Gene Myopathy, Early-Onset Genetic Test TEST-5239 LOINC 82939-0 This test performs full gene sequencing of MEGF10 to detect mutations causing early-onset myopathy (EMARDD). Peripheral whole blood, extracted DNA, or FTA card 3–4 weeks 2,800.00 AED Details
MYF6 Gene Centronuclear Myopathy Type 3 Genetic Test TEST-4002 LOINC 55233-1 This test identifies pathogenic variants within the MYF6 gene associated with Centronuclear Myopathy Type 3. Whole Blood (Peripheral) 3–4 Weeks 2,800.00 AED Details
MYH7 Gene Myosin Storage Myopathy Genetic Test TEST-5370 LOINC 78520-7 This test identifies pathogenic variants in the MYH7 gene associated with myosin storage myopathy. Whole blood (EDTA) or DNA (FTA card) 3–4 Weeks 2,800.00 AED Details
RYR1 Gene Central Core Disease Genetic Test TEST-3989 LOINC 82319-9 This test evaluates the RYR1 gene for variants associated with Central Core Disease and malignant hyperthermia susceptibility. Peripheral whole blood (3–5 mL in EDTA tube) or FTA card spot 3–4 weeks from sample receipt 2,800.00 AED Details
SCN4A Gene Myasthenic Syndrome Genetic Test TEST-5289 LOINC 81247-9 This genetic test evaluates the SCN4A gene for mutations associated with congenital myasthenic syndrome. Whole Blood, Extracted DNA, or FTA Card 3–4 Weeks 2,800.00 AED Details
Spino‑Bulbar Muscular Atrophy (SBMA) Genetic Test TEST-3154 LOINC 21666-9 This test evaluates the androgen receptor (AR) gene for CAG repeat expansions, which are characteristic of Spino-Bulbar Muscular Atrophy (Kennedy dise... Whole Blood (EDTA) 5 Working Days 1,800.00 AED Details

Clinical overview

About Neuromuscular Genetics

Understanding the broader hereditary factors affecting muscle and nerve integrity empowers families to access proactive, specialized care when symptoms are complex or ambiguous. Integrated into our advanced Genetics department, comprehensive Neuromuscular Genetics screening utilizes multi-gene panels to simultaneously evaluate a wide spectrum of hereditary pathways linked to various limb-girdle dystrophies, motor neuron diseases, and myopathies. Utilizing state-of-the-art genomic profiling, this robust screening uncovers elusive genetic drivers, offering the exact clarity required to safely guide specialized multidisciplinary neurological care, proactive respiratory monitoring, and customized early intervention physical therapies. Highly regarded for clinical excellence among diagnostic labs in Dubai and the UAE, DNA Labs ensures absolute patient confidentiality, unparalleled diagnostic accuracy, and remarkably fast turnaround times. Empower your customized medical care journey—book your neuromuscular genetics testing in UAE, arrange a secure clinical sample transfer, or consult our expert neurogenetics professionals today.

Before your appointment

Preparation & sample collection

Follow the instructions you are given

Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.

Bring your identification

A valid photo ID is required at collection so that your sample is matched correctly to your record.

Tell us about medicines

Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.

Ask before collection

If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.

Patient information

Frequently asked questions

Practical answers about Neuromuscular Genetics testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.

How do I choose the right Neuromuscular Genetics test?

The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.

What specimen is required?

Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.

Do you offer home sample collection in Dubai and the UAE?

Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.

How long do results take?

Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.

Is there anything I need to do before sample collection?

Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.

How will I receive my report?

Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.

About this clinical information

The information on this Neuromuscular Genetics page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.

  • Investigation names, specimen types and listed prices are reviewed against laboratory records.
  • Preparation guidance is indicative — confirm test-specific instructions before collection.
  • Content is updated when investigations, methods or reporting formats change.
  • Results are released to the patient and, on request, shared with the referring clinician.

Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.

We're here to help

Need help choosing a Neuromuscular Genetics test?

Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.

Call +971 54 548 8731
  • Home collection available across the UAE
  • Digital reports delivered securely
  • Confidential handling of every request

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