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    Fragile X Methylation Study

    About This Test

    The Fragile X Methylation Study is a specialized genetic test that evaluates the FMR1 gene on the X chromosome to diagnose Fragile X Syndrome (FXS), the most common inherited cause of intellectual disability and autism.

    Sample TypeSample Type
    OTHER
    iconResults
    N/A
    iconFasting
    Fasting is not required
    iconPrice
    Starting ₹0
    Age Category
    18-60
    Who Should Book This Test?

    Pediatricians / Developmental specialists For children with developmental delay, speech delay, or intellectual disability. Neurologists / Psychiatrists For patients with autism spectrum disorder, ADHD, or behavioral issues of unclear cause. Medical Geneticists / Genetic Counselors For diagnosis, carrier screening, or family planning. Obstetricians / Fertility Specialists If carrier screening is needed in couples with a family history of Fragile X or unexplained infertility.

    Sabhi Labs, Sahi Price
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