Detects deletions in exon 7 of the SMN1 gene, responsible for spinal muscular atrophy (SMA)…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
Spinal Muscular Atrophy (SMA) Molecular Analysis
11,235 THB
SKU :
MD-NLM224
Detects deletions in exon 7 of the SMN1 gene, responsible for spinal muscular atrophy (SMA).
Lab Categories : Children, EDTA Blood, Genetic Disorder, Infants, Lab Test, Muscle Weakness, PCR & Capillary Electrophoresis, Spinal Muscular Atrophy
Diseases : Spinal Muscular Atrophy
Symptoms : Muscle Weakness
Habits : Genetic Disorder
Specimens : EDTA Blood
Diagnostic Methods : PCR & Capillary Electrophoresis
| Also Known As | SMA Genetic Test |
|---|---|
| Specimen | EDTA blood 3 ml |
| Turnaround Time | 14 days |
| Test Code | MD-NLM224 |
| Test Type | Special |
| Related Tests | Neuromuscular Disorder Panel |
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