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Fragile X Syndrome

Identify a genetic cause of intellectual disability and autism to get early support and treatment

  • 15 minutes
  • 410 British pounds
  • 305 Neasden Lane, London NW10 1QR, UK

Service Description

PCR Fragile X syndrome (FXS) is a genetic disorder. FXS is caused by changes in a gene called Fragile X Messenger Ribonucleoprotein 1 (FMR1). FMR1 usually makes a protein called FMRP that is needed for brain development. People who have FXS do not make this protein. FXS affects both males and females. However, females often have milder symptoms than males. Sample: BLOOD Results: 2-3 WEEKS Phlebotomy fee: Included in price


Cancellation Policy

To cancel or schedule, please contact us 24 hours in advance


Contact Details

  • 305 Neasden Lane, London NW10 1QR, UK

    02071268511

    info@ejbio.co.uk


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