Detects mutations in the GLA gene associated with Fabry disease using next-generation sequencing (NGS)…. 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.
Fabry disease (GLA)(LMGG)
24,192 THB
SKU :
MD-NLMM523
Detects mutations in the GLA gene associated with Fabry disease using next-generation sequencing (NGS).
Lab Categories : All Ages, EDTA Whole Blood, Fabry Disease, Genetic Disorder, Kidney Failure, Lab Test, NGS (Next-Generation Sequencing), Pain
Diseases : Fabry Disease
Symptoms : Kidney Failure, Pain
Habits : Genetic Disorder
Age Groups : All Ages
Specimens : EDTA Whole Blood
Diagnostic Methods : NGS (Next-Generation Sequencing)
| Also Known As | Fabry Disease Genetic Test |
|---|---|
| Specimen | EDTA blood 6 ml |
| Turnaround Time | 1 month |
| Test Code | MD-NLMM523 |
| Test Type | Special |
| Related Tests | Lysosomal Storage Disorders Panel |
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