Cargando…
Do people with hereditary cancer syndromes inform their at-risk relatives? A systematic review and meta-analysis
PURPOSE: To evaluate rates of familial disclosure of hereditary cancer syndrome information. METHODS: A systematic review and meta-analysis was conducted in accordance with PRISMA guidelines (PROSPERO no.: CRD42020134276). Key electronic databases were searched to identify studies evaluating heredit...
Autores principales: | Ahsan, Muhammad Danyal, Levi, Sarah R., Webster, Emily M., Bergeron, Hannah, Lin, Jenny, Narayan, Priyanka, Nelson, Becky Baltich, Li, Xuan, Fowlkes, Rana K., Brewer, Jesse T., Thomas, Charlene, Christos, Paul J., Chapman-Davis, Eloise, Cantillo, Evelyn, Holcomb, Kevin, Sharaf, Ravi N., Frey, Melissa K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194207/ https://www.ncbi.nlm.nih.gov/pubmed/37214514 http://dx.doi.org/10.1016/j.pecinn.2023.100138 |
Ejemplares similares
-
Applying the framework for developing and evaluating complex interventions to increase family communication about hereditary cancer
por: Cragun, Deborah L., et al.
Publicado: (2023) -
Evaluation of an educational conference for persons affected by hereditary frontotemporal degeneration and amyotrophic lateral sclerosis
por: Dratch, Laynie, et al.
Publicado: (2022) -
Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study
por: Walters, Nicole L., et al.
Publicado: (2023) -
Investigation of interest in and timing preference for cancer predisposition testing and expanded carrier screening among women of reproductive age
por: Zhong, Lingzi, et al.
Publicado: (2023) -
Development of a novel measure of advanced cancer patients’ perceived utility of secondary germline findings from tumor genomic profiling
por: Hamilton, Jada G., et al.
Publicado: (2023)