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Spinal muscular atrophy carrier screening with Fragile X syndrome analysis

฿13,300.00

Additional information

Also Known As

SMA/Fragile X Carrier Screening
Specimen

EDTA whole blood 3 mL 2 tube
Turnaround Time

10 Days
Test Code

MD-NLM229
Test Type

Special
Related Tests

SMA Gene Testing, Fragile X Gene Testing
Product tags: Developmental Delays, Fragile X Syndrome, Genetic Disorders, Muscle Weakness, None, SMA/Fragile X Carrier Screening, Spinal Muscular Atrophy (SMA)
Diseases: Fragile X Syndrome, Genetic Disorders, Spinal Muscular Atrophy (SMA)
Symptoms: Developmental Delays, Muscle Weakness
Habits: None
Age Groups: Pediatrics, Prenatal
Specimens: EDTA Whole Blood
Diagnostic Methods: Real-time PCR, RP-PCR

Description

A carrier screening test that assesses the risk for spinal muscular atrophy (SMA) and Fragile X syndrome, two genetic conditions. Early detection is important for family planning and disease management.

Additional information

Also Known As

SMA/Fragile X Carrier Screening
Specimen

EDTA whole blood 3 mL 2 tube
Turnaround Time

10 Days
Test Code

MD-NLM229
Test Type

Special
Related Tests

SMA Gene Testing, Fragile X Gene Testing

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