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
7 Diagnostic Centers found for RETT SYNDROME DETECTION in Chandigarh
  • SCO-38, Sector 19 D, Chandigarh-160019


    0172 5019886

    psc.chandigarh2@lalpathlabs.com

    Collection Center
  • Booth No. 343, Sector 32 D, Chandigarh-160032


    9953972272, 9953959260

    psc.chandigarh@lalpathlabs.com

    Collection Center
  • SCO No 81, Sector 38 C, Chandigarh-160036


    0172 5019887

    psc.chandigarh4@lalpathlabs.com

    Collection Center
  • SCO-361,Sec-44D, Chandigarh-160047


    9953983928

    psc.chandigarh3@lalpathlabs.com

    Collection Center
  • SHOP NO 12-A ADJOINING BSNL TELEPHONE EXCHANGE GOVIND VIHAR BALTANA


    0176 2509300, 8054113020

    PSC.BALTANA@LALPATHLABS.COM

    Collection Center
  • Booth No.-31, Sector 47C, Chandigarh-160047


    0172 5034135

    psc.chandigarh47@lalpathlabs.com

    Collection Center
  • Booth No-100, Sector-38C, Chandigarh-160036


    0172-5019887

    Psc.chandigarh4@lalpathlabs.com

    Collection Center