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Diagnostic options · UAE

Limb-Girdle Muscular Dystrophy tests in Dubai & UAE

Compare available Limb-Girdle Muscular Dystrophy tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

3

Listed price range

2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Limb-Girdle Muscular Dystrophy test prices

Showing 1–3 of 3 matching tests.

Limb-Girdle Muscular Dystrophy diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-4831
ANO5 Gene Limb‑Girdle Muscular Dystrophy Type 2L (LGMD2L) Genetic Test

This test detects pathogenic variants in the ANO5 gene, providing a definitive diagnosis for autosomal recessive Limb-Girdle Muscular Dystrophy Type 2L (LGMD2L).

Whole Blood (2 mL) 3–4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["ANO5 gene sequence", "Copy Number Variants (CNVs) in ANO5 gene"]
Parameters
[]
Preparation
["No specific fasting required", "Inform lab of any medications"]
Indications
["Clinical suspicion of LGMD2L", "Family history of LGMD2L", "Need for definitive diagnosis for management and family planning"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 85047-9 ICD-10: G71.0
Clinical summary
This test detects pathogenic variants in the ANO5 gene, providing a definitive diagnosis for autosomal recessive Limb-Girdle Muscular Dystrophy Type 2L (LGMD2L).
TEST-4719
POMK Gene Limb‑Girdle Muscular Dystrophy Type 12C Genetic Test

This diagnostic test evaluates the POMK gene for pathogenic variants associated with limb-girdle muscular dystrophy type 12C (LGMDR12).

Peripheral whole blood (EDTA tube) or buccal swab (DNA FTA card) 3–4 weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the POMK gene", "Single-nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy-number variants (CNVs)"]
Parameters
[]
Preparation
["No specific fasting required.", "Inform the phlebotomist of any medications you are taking."]
Indications
["Clinical suspicion of limb-girdle muscular dystrophy type 12C", "Family history of LGMDR12", "Need for definitive genetic diagnosis for treatment planning and genetic counseling"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82128-5 ICD-10: G71.0, Z13.7, Z82.79
Clinical summary
This diagnostic test evaluates the POMK gene for pathogenic variants associated with limb-girdle muscular dystrophy type 12C (LGMDR12).
TEST-4824
TRIM32 Gene Limb‑Girdle Muscular Dystrophy Autosomal Recessive Type 2H Genetic Test

This genetic test screens the TRIM32 gene for pathogenic variants associated with autosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H).

Peripheral whole blood (3–5 mL in EDTA tube), extracted DNA, or dried blood spot (FTA card). 3–4 weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the TRIM32 gene", "Coding region and splice sites of TRIM32"]
Parameters
[]
Preparation
["No fasting required", "No medication changes required", "Pre-genetic counselling session mandatory"]
Indications
["Suspected diagnosis of Limb-Girdle Muscular Dystrophy Type 2H", "Family history of LGMD2H", "Genetic counselling for at-risk relatives"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 49733-2 ICD-10: G71.03, G71.0
Clinical summary
This genetic test screens the TRIM32 gene for pathogenic variants associated with autosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H).

Category overview

Limb-Girdle Muscular Dystrophy: overview

Experiencing progressive muscle weakness in the shoulders or hips can profoundly impact your daily life, but pinpointing the underlying molecular cause is the first step toward relief and reassurance. Within our Molecular Diagnostics division, our advanced Limb-Girdle Muscular Dystrophy testing uses cutting-edge DNA sequencing to uncover the complex inherited genetic factors affecting your muscle integrity. Rather than providing a standalone clinical diagnosis, this precise genetic data empowers your neurologist with the crucial insights needed for tailored, proactive medical guidance and supportive management. As one of the leading diagnostic labs in Dubai and the UAE, DNA Labs UAE ensures rigorous patient confidentiality and rapid, highly accurate turnaround times. Take charge of your neuromuscular health: explore our limb-girdle muscular dystrophy testing in the UAE below to book your appointment, schedule a convenient home sample collection, or consult our specialized medical team.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.