Clinical

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Pancreatic Cancer Screening of High-Risk Individuals in Arkansas


ABSTRACT: 100 subjects who have a family history of pancreatic cancer (PC), or known genetic syndromes associated with increased risk of pancreatic cancer, will be followed for five years. This data will be used to determine the pancreatic cancer and precancerous lesion detection rate in High Risk Individuals (HRIs). Subjects may agree to annual imaging and annual biomarkers or to biomarkers only.

DISEASE(S): Dysplastic Nevus Syndrome,Ataxia Telangiectasia,Brca2 Gene Mutation,Pancreatitis, Chronic,Pancreatitis,Hereditary Pancreatitis,Melanoma,Familial Atypical Mole-malignant Melanoma Syndrome,Brca1 Gene Mutation,Colorectal Neoplasms, Hereditary Nonpolyposis,Neoplasms,Telangiectasis,Peutz-jeghers Syndrome,Colorectal Neoplasms,Pancreatic Neoplasms,Peutz-jegher's Syndrome

PROVIDER: 2179717 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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