PRADER-WILLI SYNDROME MUTATION DETECTION, METHYLATION SPECIFIC PCR

  • Test Usage:
    Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are clinically distinct neurodevelopmental genetic disorders that map to 15q11-q13. The primary phenotypes are attributable to loss of expression of imprinted genes within this region which can arise by means of a number of mechanisms. The most sensitive single approach to diagnosing both PWS and AS is to study methylation patterns within 15q11-q13
  • Report Availability:
    Sample by Sat 11 am; Report 12 days
14 Diagnostic Centers found for PRADER-WILLI SYNDROME MUTATION DETECTION, METHYLATION SPECIFIC PCR in Jodhpur