ANGELMAN SYNDROME

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

  • Test Type:
  • Pre-test Information:
    No Special preparation required
  • Report Delivery:
    Sample by Sat 11 am; Report 12 days
  • Components:
    0