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Fragile X Syndrome Genetic Test

Qatar, Doha Since 2000 0 (0 reviews) Share Now 5 Views

This genetic test evaluates Fragile X syndrome mutations to help diagnose inherited developmental and intellectual disorders and identify carrier status.

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Accredited Facility E-report Qualified Specialists

This genetic test detects mutations in the FMR1 gene associated with Fragile X syndrome. It helps diagnose Fragile X syndrome and identify carriers.

  • If developmental delay or intellectual disability is present.
  • During evaluation of autism spectrum or behavioral disorders.
  • When family history of Fragile X syndrome exists.
  • For carrier screening before pregnancy.As part of genetic counseling or assessment.
  • No fasting is usually required.
  • A blood sample or cheek swab may be collected.
  • Genetic counseling may be recommended before and after testing.
  • Inform the healthcare provider about family history of genetic disorders.
  • Follow all laboratory instructions before sample collection.
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    Starting From

    QR1,850.00

    Accredited Facility
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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

    202

    Location