Muscular Dystrophy Genetics tests in Dubai & UAE

Compare available Muscular Dystrophy Genetics 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

1,800.00–2,800.00 AED

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Muscular Dystrophy Genetics test prices

Showing 1–5 of 5 matching tests.

Muscular Dystrophy Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5162 CAPN3 Gene Limb‑Girdle Muscular Dystrophy Type 2A (LGMD2A) Genetic Test This genetic test identifies pathogenic variants within the CAPN3 gene, which are responsible for causing Limb-Girdle Muscular Dystrophy Type 2A.	Whole Blood (EDTA) – 5 mL	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 CAPN3 gene"] Parameters [] Preparation [] Indications ["Confirming clinical suspicion of LGMD2A", "Carrier screening", "Family planning decisions"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: G71.0 Clinical summary This genetic test identifies pathogenic variants within the CAPN3 gene, which are responsible for causing Limb-Girdle Muscular Dystrophy Type 2A.
TEST-1034 Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test This diagnostic test evaluates the dystrophin gene for deletions and duplications, which are common causes of Duchenne and Becker muscular dystrophies.	Peripheral whole blood	21 calendar days (3 weeks)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Dystrophin gene deletions", "Dystrophin gene duplications"] Parameters [] Preparation ["No special preparation required", "Standard blood sample collection"] Indications ["Suspected diagnosis of DMD or BMD", "Family history of DMD or BMD", "Carrier screening for female relatives", "Pre-implantation genetic diagnosis (PGD)", "Eligibility assessment for gene therapy"] Measurement technique Confirm with laboratory Codes LOINC: 21655-8 ICD-10: G71.0 Clinical summary This diagnostic test evaluates the dystrophin gene for deletions and duplications, which are common causes of Duchenne and Becker muscular dystrophies.
TEST-2726 Nx Gen Sequencing: Duchenne & Becker Muscular Dystrophy Test This test identifies pathogenic variants in the dystrophin gene (DMD) associated with Duchenne and Becker muscular dystrophies.	Whole Blood	40 Working Days	2,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the DMD gene", "Dystrophin gene sequence"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Ensure Whole Exome Sequencing Consent Form (Form 37) is signed"] Indications ["Clinical suspicion of Duchenne Muscular Dystrophy (DMD)", "Clinical suspicion of Becker Muscular Dystrophy (BMD)", "Family history of DMD or BMD", "Elevated CK levels without clear diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94223-0 ICD-10: G71.01, G71.02 Clinical summary This test identifies pathogenic variants in the dystrophin gene (DMD) associated with Duchenne and Becker muscular dystrophies.
TEST-4839 POMT1 Gene Limb-Girdle Muscular Dystrophy (LGMD2N) Genetic Test This test identifies disease-causing mutations in the POMT1 gene to confirm or exclude a diagnosis of LGMD2N.	Whole Blood (Peripheral Venous Sample)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["POMT1 gene sequence", "Copy Number Variants (CNVs) in POMT1"] Parameters [] Preparation ["No fasting required", "No dietary restriction required", "No special preparation required"] Indications ["Confirmation of LGMD2N diagnosis", "Family screening for at-risk relatives", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 94121-5 ICD-10: G71.0 Clinical summary This test identifies disease-causing mutations in the POMT1 gene to confirm or exclude a diagnosis of LGMD2N.
TEST-4731 TCAP Gene Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2) Genetic Test This genetic test analyzes the TCAP gene to identify pathogenic variants associated with Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2).	Peripheral Whole Blood, Dried Blood Spot, or DNA Sample	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TCAP gene coding region", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions"] Indications ["Clinical suspicion of Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2)", "Family history of LGMDR2", "Carrier screening for relatives"] Measurement technique Confirm with laboratory Codes LOINC: 81247-5 ICD-10: G71.0 Clinical summary This genetic test analyzes the TCAP gene to identify pathogenic variants associated with Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2).

Category overview

Muscular Dystrophy Genetics: overview

Understanding the broader hereditary factors affecting muscle integrity empowers families to access proactive, specialized care when symptoms are complex or ambiguous. Integrated into our advanced Genetics department, comprehensive Muscular Dystrophy Genetics screening utilizes multi-gene panels to simultaneously evaluate a wide spectrum of hereditary pathways linked to various limb-girdle and congenital muscular dystrophies. 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 cardiac 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 muscular dystrophy genetics testing in UAE, arrange a secure clinical sample transfer, or consult our expert neurogenetics professionals today.

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