Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Arkansas
Age
18–99
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Have a family history of PC as listed below or who have one of the following syndromes: Peutz-Jeghers syndrome - STK11; BRCA 1 and 2; PALB2; ATM; FAMMM / P16; HNPCC (Lynch) / MMR genes; Hereditary pancreatitis - PRSS1
Individuals with three or more affected blood relatives (1st, 2nd or 3rd degree)
Individuals with two or more affected blood relatives with PC, with at least one affected FDR, should be considered for screening.
Patients with a history of Peutz-Jeghers syndrome should be screened, regardless of family history of PC.
Patients with a known p16 (FAMMM syndrome) with one affected 1st or 2nd degree relative will be considered for screening.
Patients with a known BRCA1 or BRCA2 mutation with one affected 1st or 2nd degree relative should be considered for screening.
Patients with a known PALB2 mutation with one affected family member should be considered for screening.
Patients with a known Mismatch-repair gene-mutation carriers (Lynch syndrome) with one affected family member should be considered for screening.
