Juvenile Polyposis Syndrome
What's New
Last Posted: Feb 16, 2023
- Genetic Predisposition to Colorectal Cancer: How Many and Which Genes to Test?
Francesca Rebuzzi et al. International journal of molecular sciences 2023 24(3) - Re-recognition of BMPR1A-related polyposis: beyond juvenile polyposis and hereditary mixed polyposis syndrome.
Zhao Zi-Ye et al. Gastroenterology report 2023 11goac082 - Management of Juvenile Polyposis Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group.
Cohen Shlomi et al. Journal of pediatric gastroenterology and nutrition 2019 68(3) 453-462 - Hereditary Gastrointestinal Cancer Syndromes: Role of Imaging in Screening, Diagnosis, and Management.
Katabathina Venkata S et al. Radiographics : a review publication of the Radiological Society of North America, Inc 2019 Aug 180185 - Systematic screening in hereditary hemorrhagic telangiectasia: a review.
Kroon Steven et al. Current opinion in pulmonary medicine 2018 24(3) 260-268 - CLINGEN Actionability Report for Hereditary Hemorrhagic Telangiectasia - ENG, ACVRL1, SMAD4, GDF2
ClinGen Actionability Working Group - CLINGEN Actionability Report for Juvenile polyposis syndrome - SMAD4, BMPR1A
ClinGen Actionability Working Group - Hereditary gastrointestinal carcinomas and their precursors: An algorithm for genetic testing.
Spoto Clothaire P E et al. Seminars in diagnostic pathology 2018 Jan - ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Syngal Sapna et al. The American journal of gastroenterology 2015 Feb 110(2) 223-62; quiz 263 - Juvenile polyposis syndrome
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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:Feb 1, 2023
- Page last updated:Jun 09, 2023
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