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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...

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Detalles Bibliográficos
Autores principales: Jelsig, Anne Marie, Karstensen, John Gásdal, Jespersen, Niels, Ketabi, Zohreh, Lautrup, Charlotte, Rønlund, Karina, Sunde, Lone, Wadt, Karin, Thorlacius-Ussing, Ole, Qvist, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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
Descripción
Sumario: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.