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Danish guidelines for management of non-APC-associated hereditary polyposis syndromes
Hereditary Polyposis Syndromes are a group of rare, inherited syndromes characterized by the presence of histopathologically specific or numerous intestinal polyps and an increased risk of cancer. Some polyposis syndromes have been known for decades, but the development in genetic technologies has a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8499431/ https://www.ncbi.nlm.nih.gov/pubmed/34620187 http://dx.doi.org/10.1186/s13053-021-00197-8 |
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author | Jelsig, Anne Marie Karstensen, John Gásdal Jespersen, Niels Ketabi, Zohreh Lautrup, Charlotte Rønlund, Karina Sunde, Lone Wadt, Karin Thorlacius-Ussing, Ole Qvist, Niels |
author_facet | Jelsig, Anne Marie Karstensen, John Gásdal Jespersen, Niels Ketabi, Zohreh Lautrup, Charlotte Rønlund, Karina Sunde, Lone Wadt, Karin Thorlacius-Ussing, Ole Qvist, Niels |
author_sort | Jelsig, Anne Marie |
collection | PubMed |
description | Hereditary Polyposis Syndromes are a group of rare, inherited syndromes characterized by the presence of histopathologically specific or numerous intestinal polyps and an increased risk of cancer. Some polyposis syndromes have been known for decades, but the development in genetic technologies has allowed the identification of new syndromes.. The diagnosis entails surveillance from an early age, but universal guideline on how to manage and surveille these new syndromes are lacking. This paper represents a condensed version of the recent guideline (2020) from a working group appointed by the Danish Society of Medical Genetics and the Danish Society of Surgery on recommendations for the surveillance of patients with hereditary polyposis syndromes, including rare polyposis syndromes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13053-021-00197-8. |
format | Online Article Text |
id | pubmed-8499431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84994312021-10-08 Danish guidelines for management of non-APC-associated hereditary polyposis syndromes Jelsig, Anne Marie Karstensen, John Gásdal Jespersen, Niels Ketabi, Zohreh Lautrup, Charlotte Rønlund, Karina Sunde, Lone Wadt, Karin Thorlacius-Ussing, Ole Qvist, Niels Hered Cancer Clin Pract Review Hereditary Polyposis Syndromes are a group of rare, inherited syndromes characterized by the presence of histopathologically specific or numerous intestinal polyps and an increased risk of cancer. Some polyposis syndromes have been known for decades, but the development in genetic technologies has allowed the identification of new syndromes.. The diagnosis entails surveillance from an early age, but universal guideline on how to manage and surveille these new syndromes are lacking. This paper represents a condensed version of the recent guideline (2020) from a working group appointed by the Danish Society of Medical Genetics and the Danish Society of Surgery on recommendations for the surveillance of patients with hereditary polyposis syndromes, including rare polyposis syndromes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13053-021-00197-8. BioMed Central 2021-10-07 /pmc/articles/PMC8499431/ /pubmed/34620187 http://dx.doi.org/10.1186/s13053-021-00197-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Jelsig, Anne Marie Karstensen, John Gásdal Jespersen, Niels Ketabi, Zohreh Lautrup, Charlotte Rønlund, Karina Sunde, Lone Wadt, Karin Thorlacius-Ussing, Ole Qvist, Niels Danish guidelines for management of non-APC-associated hereditary polyposis syndromes |
title | Danish guidelines for management of non-APC-associated hereditary polyposis syndromes |
title_full | Danish guidelines for management of non-APC-associated hereditary polyposis syndromes |
title_fullStr | Danish guidelines for management of non-APC-associated hereditary polyposis syndromes |
title_full_unstemmed | Danish guidelines for management of non-APC-associated hereditary polyposis syndromes |
title_short | Danish guidelines for management of non-APC-associated hereditary polyposis syndromes |
title_sort | danish guidelines for management of non-apc-associated hereditary polyposis syndromes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8499431/ https://www.ncbi.nlm.nih.gov/pubmed/34620187 http://dx.doi.org/10.1186/s13053-021-00197-8 |
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