Muscular Dystrophy Genetic tests in Dubai & UAE

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

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Listed price range

2,800.00 AED

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Muscular Dystrophy Genetic test prices

Showing 1–7 of 7 matching tests.

Muscular Dystrophy Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5842 COL6A3 Gene Sequencing (Ullrich Congenital Muscular Dystrophy Type 1) Genetic Test This test evaluates the COL6A3 gene for pathogenic variants associated with Ullrich congenital muscular dystrophy type 1.	Whole blood, extracted DNA, or FTA card (peripheral blood)	3–4 Weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["COL6A3 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [{"name": "Analytical Sensitivity", "reference_range": "99.9% for single nucleotide variants and small indels"}] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Ullrich congenital muscular dystrophy type 1", "Family history of collagen VI-related myopathies"] Measurement technique Confirm with laboratory Codes LOINC: 78025-3 ICD-10: G71.0, G71.2 Clinical summary This test evaluates the COL6A3 gene for pathogenic variants associated with Ullrich congenital muscular dystrophy type 1.
TEST-5253 LMNA Gene Congenital Muscular Dystrophy NGS Test This test identifies pathogenic variants in the LMNA gene, which are associated with congenital muscular dystrophy and other laminopathies.	Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LMNA gene sequence", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number changes"] Parameters [] Preparation [] Indications ["Clinical suspicion of LMNA-related congenital muscular dystrophy", "Family history of laminopathy", "Need for genetic confirmation for diagnosis and management"] Measurement technique Confirm with laboratory Codes LOINC: 94477-1 ICD-10: G71.00 Clinical summary This test identifies pathogenic variants in the LMNA gene, which are associated with congenital muscular dystrophy and other laminopathies.
TEST-5260 PLEC Gene Muscular Dystrophy, Limb‑Girdle, Type 2Q Genetic Test This test identifies pathogenic variants in the PLEC gene associated with Limb-Girdle Muscular Dystrophy Type 2Q.	Whole blood (EDTA), extracted DNA, or FTA card blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Biallelic mutations in the PLEC gene", "Copy Number Variations (CNV) in the PLEC gene"] Parameters [] Preparation ["No special preparation needed", "Maintain normal hydration", "Inform phlebotomist if on anticoagulants"] Indications ["Diagnosis of suspected LGMD2Q", "Carrier screening for at-risk family members", "Prognostic insight for affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82162-1 ICD-10: G71.0 Clinical summary This test identifies pathogenic variants in the PLEC gene associated with Limb-Girdle Muscular Dystrophy Type 2Q.
TEST-4740 POMT1 Gene Sequencing for Limb-Girdle Muscular Dystrophy Type 2K (Autosomal Recessive) Test This test evaluates the POMT1 gene for mutations associated with Limb-Girdle Muscular Dystrophy Type 2K (LGMD2K). It uses Next-Generation Sequencing (NGS) to analyze the entire cod...	Whole blood (venous puncture) or FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["POMT1 gene mutations", "Pathogenic variants in POMT1"] Parameters [] Preparation ["No specific fasting required", "Avoid blood transfusion within the last 8 weeks"] Indications ["Clinical suspicion of Limb-Girdle Muscular Dystrophy Type 2K", "Family history of LGMD2K"] Measurement technique Confirm with laboratory Codes LOINC: 81309-2 ICD-10: G71.0 Clinical summary This test evaluates the POMT1 gene for mutations associated with Limb-Girdle Muscular Dystrophy Type 2K (LGMD2K). It uses Next-Generation Sequencing (NGS) to analyze the entire coding region.
TEST-5264 RXYLT1 Gene Muscular Dystrophy‑Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A10 Genetic Test This test identifies pathogenic variants in the RXYLT1 gene associated with Muscular Dystrophy-Dystroglycanopathy Type A10 (MDDGA10).	Whole blood (EDTA) or buccal swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RXYLT1 gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Suspicion of MDDGA10", "Walker-Warburg syndrome phenotype", "Carrier testing in at-risk family members", "Prenatal genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81209-4 ICD-10: G71.0 Clinical summary This test identifies pathogenic variants in the RXYLT1 gene associated with Muscular Dystrophy-Dystroglycanopathy Type A10 (MDDGA10).
TEST-4821 SGCB Gene Limb‑Girdle Muscular Dystrophy Autosomal Recessive Type 2E (LGMD2E) Genetic Test This genetic test identifies disease-causing mutations within the SGCB gene, associated with autosomal recessive limb-girdle muscular dystrophy type 2E.	Whole blood, extracted DNA, or FTA card	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SGCB gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)"] Parameters [] Preparation ["Provide detailed clinical history", "Attend pre-test genetic counselling session"] Indications ["Suspected LGMD2E diagnosis", "Family history of autosomal recessive myopathy", "Carrier testing", "Prenatal decision-making"] Measurement technique Confirm with laboratory Codes LOINC: 76992-0 ICD-10: G71.0 Clinical summary This genetic test identifies disease-causing mutations within the SGCB gene, associated with autosomal recessive limb-girdle muscular dystrophy type 2E.
TEST-4808 SGCD Gene Limb‑Girdle Muscular Dystrophy Type 2F Genetic Test This genetic test identifies biallelic mutations in the SGCD gene, confirming a diagnosis of Limb-Girdle Muscular Dystrophy Type 2F.	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA® card)	3 – 4 weeks (standard)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SGCD gene coding exons", "Flanking splice sites"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist about anticoagulant use"] Indications ["Suspected LGMD2F based on clinical symptoms", "Family history of LGMD2F", "Elevated creatine kinase levels", "Carrier detection", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 95193-8 ICD-10: G71.0 Clinical summary This genetic test identifies biallelic mutations in the SGCD gene, confirming a diagnosis of Limb-Girdle Muscular Dystrophy Type 2F.

Category overview

Muscular Dystrophy Genetic: overview

When clinical signs strongly point to a specific neuromuscular breakdown, getting a targeted genetic confirmation is the key to unlocking the safest, most effective long-term management and reproductive confidence. As a highly focused diagnostic tool in our Molecular Genetics services, Muscular Dystrophy Genetic testing specifically targets the exact DNA mutations—such as deletions in the DMD gene—responsible for your family's unique presentation. By leveraging advanced sequencing and deletion/duplication analysis, this precise genomic screening provides the definitive data necessary to assess disease severity, evaluate carrier risks for future children, and safely guide customized pediatric and adult neurology care. Consistently trusted by neurologists across the top diagnostic labs in the UAE, DNA Labs guarantees strict patient confidentiality, exceptional analytical precision, and incredibly efficient reporting. Protect your family's mobility—schedule your muscular dystrophy genetic testing in UAE, coordinate a comfortable home sample collection, or connect with our specialized genetic counselors.

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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.