FRAGILE X MUTATION & CHROMOSOMAL ARRAY PROFILE

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NABL Cap Accredited    
The Fragile X Mutation and Chromosomal Array Profile by Metropolis Healthcare evaluates genetic variations associated with Fragile X syndrome and other chromosomal abnormalities. It detects CGG repeat expansions in the FMR1 gene along with copy number variations across the genome. This comprehensive analysis helps in early diagnosis of intellectual disability, developmental delays, and reproductive counseling. Metropolis Healthcare provides accurate and reliable genetic testing using advanced molecular and array-based technologies

  • 17 Crores+ Samples Processed
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  • Free Home Collection

Price: Rs. 22,050.00

Sample Type: EDTA Blood

Fasting Not Required


Notes: F0117

Frequently Asked Questions (FAQ's):

What does the Fragile X & Chromosomal Array Profile test detect?
It identifies FMR1 gene mutations and chromosomal abnormalities using Metropolis Healthcare’s advanced molecular and array techniques.

Why is this test important?
It helps diagnose Fragile X syndrome, developmental delays, and other genetic conditions early.

What sample is required?
An EDTA blood sample is collected for DNA extraction and analysis.

Who should take this test?
Individuals with intellectual disability, developmental delays, autism spectrum disorder, or those seeking reproductive genetic counseling.

Is fasting required?
No fasting is necessary for this genetic test.

How long do results take at Metropolis Healthcare?
Results are usually available within 2–3 weeks depending on testing complexity.

How do the results help?
They guide diagnosis, early intervention, management planning, and reproductive decision-making.

Can this test detect all chromosomal disorders?
It detects a wide range of copy number variations and Fragile X mutations, but not all genetic disorders—consult your doctor for comprehensive evaluation

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