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Fragile X syndrome

฿9,600.00

Additional information

Also Known As

FMR1 Gene Test, Fragile X DNA Test, Fragile X Syndrome Screening

Specimen

EDTA whole blood 5 ml (minimum 2 ml)

Turnaround Time

2 months

Test Code

MD-NLT113

Test Type

General

Genetic testing for Fragile X syndrome, a common inherited cause of intellectual disability. Detects mutations in the FMR1 gene, particularly the expansion of CGG repeats, which is associated with the condition. Essential for diagnosis and family planning.

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Description

Genetic testing for Fragile X syndrome, a common inherited cause of intellectual disability. Detects mutations in the FMR1 gene, particularly the expansion of CGG repeats, which is associated with the condition. Essential for diagnosis and family planning.

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

FMR1 Gene Test, Fragile X DNA Test, Fragile X Syndrome Screening

Specimen

EDTA whole blood 5 ml (minimum 2 ml)

Turnaround Time

2 months

Test Code

MD-NLT113

Test Type

General