• 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 Sat by 11 am; Report 12 days
47 Diagnostic Centers found for ANGELMAN SYNDROME in Allahabad