FISH - Prader Willi Syndrome SNRPN

Most cases (99%) are caused by absence of a paternal contribution to the imprinted region on chromosome 15q11-q13; approximately 70% of these are due to a large -5-7 Mb deletion.

  • Test Type:
  • Pre-test Information:
    Duly filled Chromosome & FISH analysis Test Request Form (Form 17) is mandatory.
  • Report Delivery:
    Sample Daily by 4 pm; Report 7 Days.
  • Components:
    0

Sample Report