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New NCCN Guidelines® Now Available for Genetic/Familial High-Risk Assessment: Colorectal

The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Genetic/Familial High-Risk Assessment: Colorectal are now available as a new addition to the library of NCCN Guidelines®.

The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Colorectal were separated from the NCCN Guidelines for Colorectal Cancer Screening and have been placed under a separate cover. These NCCN Guidelines cover the following topics:

  • Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)
  • Familial Adenomatous Polyposis (FAP)
  • Attenuated Familial Adenomatous Polyposis (AFAP)
  • MUTYH-Associated Polyposis (MAP)
  • Peutz-Jeghers Syndrome (PJS)
  • Juvenile Polyposis Syndrome (JPS)
  • Serrated Polyposis Syndrome (SPS)
  • Colonic Adenomatous Polyposis of Unknown Etiology

The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Colorectal are available free-of-charge on NCCN.org