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Fragile X (FMR1) CGG Repeat Analysis Test in Dahisar
50+ booked in last 3 days
No special precautions
Sample Type
Blood
Recommended for
Male, Female
Report
Within 24 Hours
Blood test at Home
NABL & CAP Accredited Labs
Accurate & Quality Test Reports
Trusted by Leading Doctors & Hospitals
Overview
Test determines CGG repeats in the FMR1 gene to diagnose Fragile X syndrome. Test uses TP-PCR/Capillary Electrophoresis. Methylation analysis is used to distinguish between premutation and full mutation alleles.
Frequently Asked Questions
This test is done to diagnose Fragile X syndrome.
This test is offered to children with development delays, learning disabilities, social & behavioural disorders.
Test determines CGG repeats in the FMR1 gene to diagnose Fragile X syndrome (FXS). Triplet repeat primed PCR (TP-PCR) is used to detect presence or absence of pathogenically expanded allele and hence determines Premutation (Carrier state) and Full mutation (Affected) in the individual.
The FMR1 gene makes a protein called FMRP which is needed for brain development and due to the genetic defect the protein is not produced resulting in development delay, learning, social & behavioural disorders in child.
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Why Metropolis?
Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.
We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.
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