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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.