Familial Pancreatic Cancer
What's New
Last Posted: Jul 22, 2021
- A systematic review of the prevalence of germline pathogenic variants in patients with pancreatic cancer.
Astiazaran-Symonds Esteban et al. Journal of gastroenterology 2021 - Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study.
Tan Ming et al. Scandinavian journal of gastroenterology 2021 1-7 - Cancer surveillance awareness and practice among families at increased risk for pancreatic adenocarcinoma.
Everett Jessica N et al. Cancer 2021 - Familial pancreatic cancer: who should be considered for genetic testing?
Kartal Kinyas et al. Irish journal of medical science 2021 - The influence of familial pancreatic cancer on postoperative outcome in pancreatic cancer: relevance to adjuvant chemotherapy.
Tezuka Koji et al. Journal of gastroenterology 2020 Oct - Familial Pancreatic Cancer: A Critical Review.
Rahman Asad Ur et al. Critical reviews in oncogenesis 2019 24(2) 149-156 - Hereditary vs Familial Pancreatic Cancer: Associated Genetic Syndromes and Clinical Perspective.
Copur Mehmet Sitki et al. Oncology (Williston Park, N.Y.) 2020 Jun 34(6) 196-201 - Familial Pancreatic Cancer: Current Perspectives.
Llach Joan et al. Cancer management and research 2020 12743-758 - Surveillance of Individuals with a Family History of Pancreatic Cancer and Inherited Cancer Syndromes: A Strategy for Detecting Early Pancreatic Cancers.
Matsubayashi Hiroyuki et al. Diagnostics (Basel, Switzerland) 2019 Oct 9(4) - Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium.
Goggins Michael et al. Gut 2019 Oct
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Oct 1, 2021
- Page last updated:Oct 07, 2021
- Content source: