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Fragile X syndrome
SKU: MD-NLT840 Categories: , , , , , , Tags: , , ,

In Stock

Fragile X syndrome

฿11,400.00

Additional information

Also Known As

Fragile X Genetic Test
Specimen

EDTA whole blood 10 ml (minimum 6 ml)
Turnaround Time

60 days
Test Code

MD-NLT840
Test Type

Special
Related Tests

Genetic Panel

Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.

Product tags: Developmental Delay, Family History, Fragile X Genetic Test, Genetic Disorders
Diseases: Genetic Disorders
Symptoms: Developmental Delay
Habits: Family History
Age Groups: Pediatric
Specimens: Blood
Diagnostic Methods: MS-PCR + CGG Repeat Analysis
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Description

Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.

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.

Additional information

Also Known As

Specimen

Turnaround Time

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