FRAGILE X (FMR1) CGG REPEAT ANALYSIS / EDTA BLOOD

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NABL Cap Accredited      
The Fragile X (FMR1) CGG Repeat Analysis at Metropolis Healthcare measures the number of CGG repeats in the FMR1 gene to detect full mutations, premutations, or intermediate alleles. This test is essential for diagnosing Fragile X syndrome, a common inherited cause of intellectual disability and developmental delay. It also supports carrier screening, fertility assessments, and evaluation of related neurological conditions. Metropolis Healthcare uses advanced molecular platforms for precise repeat-size detection and high-quality genetic reporting

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Price: Rs. 7,315.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: F0050

Frequently Asked Questions (FAQ's):

What does the Fragile X CGG repeat test detect?
It identifies expanded CGG repeats in the FMR1 gene linked to Fragile X syndrome and carrier states.

Who should take this test?
Children with developmental delay, autism spectrum features, or individuals with a family history of Fragile X syndrome.

How does Metropolis Healthcare perform this test?
Metropolis uses sensitive molecular techniques such as PCR and reflex methods to measure CGG repeat counts accurately.

Can this test identify carriers?
Yes, it detects premutation carriers who may be asymptomatic but can transmit the mutation.

Is any preparation required?
No fasting or special preparation is needed for this EDTA blood-based test.

How reliable is this test?
Metropolis Healthcare ensures high analytical accuracy through advanced molecular genetics technology.

Can this test help in fertility assessments?
Yes, premutation carriers may have ovarian insufficiency, and this test assists in reproductive planning.

How long does it take to receive results?
Results are generally available within a few working days, depending on the complexity of analysis

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