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FMR1 Gene (Fragile X Syndrome), PCR

Qatar, Doha Since 2000 0 (0 reviews) Share Now 1 Views

This PCR-based genetic test analyzes the FMR1 gene to detect CGG repeat expansions associated with Fragile X syndrome and related inherited intellectual disability disorders.

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Accredited Facility E-report Qualified Specialists

This test evaluates the FMR1 gene for CGG repeat expansion mutations. It helps diagnose Fragile X syndrome and identify carriers at risk of transmitting the condition.

  • If intellectual disability or developmental delay is present.
  • During autism spectrum disorder evaluation.
  • When Fragile X syndrome is suspected clinically.
  • In individuals with a family history of genetic disorders.
  • As part of preconception or genetic counseling screening.
  • No fasting is required.
  • A blood sample will be collected from a vein.
  • Genetic counseling is recommended before and after testing.
  • Family history information may assist interpretation.
  • Follow all laboratory instructions before sample collection.
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    Starting From

    QR3,500.00

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    Lab Details
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    Al Arabi Laboratory & Radiology
    Lab Since

    2000

    Address

    Al Jazira Al Arabiya Street, Doha, Doha, Qatar

    Email

    admin@gulflab-xray.com

    Phone

    +97455856923

    Available Tests

    283

    Location