RETT SYNDROME DETECTION

  • Test Usage:
    Genetically, Rett syndrome (RTT) is caused by mutations in the gene MECP2 located on the X chromosome (which is involved in transcriptional silencing and epigenetic regulation of methylated DNA), and can arise sporadically or from germline mutations. In less than 10% of RTT cases, mutations in the genes CDKL5 or FOXG1 have also been found to resemble it. Rett syndrome is initially diagnosed by clinical observation, but the diagnosis is definitive when there is a genetic defect in the MECP2 gene.
  • Report Availability:
    Sample by Sat 11 am; Report 13 days
4 Diagnostic Centers found for RETT SYNDROME DETECTION in Surat
  • Shraddha Clinical Lab, 1/3821, First Floor, Desai Pole, Soni Faliya, Gopipura, Surat, Gujarat-395003


    0261 2599945, 0261 2599946, 9825052183

    shraddhalab@hotmail.com

    Collection Center
  • U-14 , AKSHAR JYOT SHOPING, NEAR MALHAR DHOSA, ADAJAN, SURAT


    9820181635, 6393628249

    devendradubey540@gmail.com

    Collection Center
  • Shop No.-U17, Ground Floor, Abhinandan Royale Complex, Opposite Rajhans Olympia, Bhatar Road, Surat, Gujarat-359001


    9898585510

    healthcarelpl@gmail.com

    Collection Center
  • G-40, Ground Floor, Sargam Doctor House, Hirabag Circle, Near Sarthi Doctor House, Varachha, Surat, Gujarat - 395006


    8866000234, 9016672667

    pareshbalar@gmail.com

    Collection Center