Diagnostic options · UAE

SMA tests in Dubai & UAE

Compare available SMA 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

Listed price range

2,000.00–2,800.00 AED

Clinical preparation

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SMA test prices

Showing 1–2 of 2 matching tests.

SMA diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5727 SMN1 Gene Sequencing (Spinal Muscular Atrophy Type 4) Genetic Test This test evaluates the SMN1 gene for mutations associated with Spinal Muscular Atrophy Type 4.	Peripheral Whole Blood, Extracted DNA, or Dried Blood Spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SMN1 gene sequence", "Point mutations", "Copy Number Variations (CNVs)", "Deep intronic variants"] Parameters [] Preparation ["Pre-genetic counselling session required", "Inform team of anticoagulant or immunosuppressant medications"] Indications ["Suspected clinical diagnosis of SMA Type 4", "Differentiation from other motor neuron diseases", "Reproductive planning for carriers"] Measurement technique Confirm with laboratory Codes LOINC: 78296-5 ICD-10: G12.1, Z14.8, Z13.79 Clinical summary This test evaluates the SMN1 gene for mutations associated with Spinal Muscular Atrophy Type 4.
TEST-3159 Spinal Muscular Atrophy (SMA) Mutation Detection Test This test detects deletions and copy number variations in the SMN1 gene, the primary cause of Spinal Muscular Atrophy (SMA). It is used for diagnosis and carrier screening.	Peripheral Whole Blood (Lavender-top EDTA Tube)	6 business days (sample submission Monday by 11 AM → report Saturday)	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SMN1 gene deletions", "SMN1 gene copy number variations"] Parameters [] Preparation ["No fasting required", "Complete Genomics Clinical Information Requisition Form (Form 20)"] Indications ["Clinical suspicion of SMA", "Family history of SMA", "Carrier screening for at-risk couples", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 36911-9 ICD-10: G12.9, G12.0, G12.1 Clinical summary This test detects deletions and copy number variations in the SMN1 gene, the primary cause of Spinal Muscular Atrophy (SMA). It is used for diagnosis and carrier screening.

Category overview

SMA: overview

Navigating concerns about motor skill development or muscle weakness in a child requires rapid, highly accurate answers to ensure the best possible supportive care. As part of our Molecular Diagnostics division, our SMA (Spinal Muscular Atrophy) testing utilizes advanced molecular sequencing to safely and conclusively evaluate mutations or deletions in the SMN1 gene. Rather than delivering a final clinical diagnosis on its own, this essential genetic data serves as a foundational tool for your pediatric neurologist, delivering the exact clarity needed to shape deeply personalized, proactive medical guidance and targeted therapies. Trusted as a leading choice among diagnostic labs in the UAE, DNA Labs UAE guarantees strict patient confidentiality alongside remarkably rapid, accurate turnaround times. Support your child’s future: explore our SMA testing in the UAE below to book an appointment, schedule a seamless home collection, or consult our specialized team.

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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.