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Pediatric Predispositional Genetic Risk Communication: Potential Utility for Prevention and Control of Melanoma Risk as an Exemplar

机译:儿科易感性遗传风险沟通:潜在的实用程序以预防和控制黑素瘤风险为例。

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摘要

Predispositional genetic testing among minor children is intensely debated due to the potential benefits and harms of providing this type of genetic information to children and their families. Existing guidelines on pediatric genetic testing state that predispositional testing could be appropriate for minors if preventive services exist that mitigate children’s risk for or severity of the health condition in question. We use the example of hereditary melanoma to illustrate the rationale for and potential application of genetic risk communication for an adult-onset cancer to a pediatric population where childhood behaviors may reduce risk of disease later in life. We draw from the adult melanoma genetic risk communication and pediatric health behavior change literatures to suggest ways in which genetic test reporting and complementary education could be delivered to children who carry a hereditary risk for melanoma and their families in order to foster children’s engagement in melanoma preventive behaviors. Genetic discoveries will continue to yield new opportunities to provide predispositional genetic risk information to unaffected individuals, including children, and could be delivered within programs that provide personalized and translational approaches to cancer prevention.
机译:由于向儿童及其家庭提供这种类型的遗传信息的潜在利弊,人们对未成年儿童的易感基因测试受到了激烈的争论。现行的儿科基因测试指南指出,如果存在预防性服务,可以减轻未成年人健康问题的风险或严重程度,则倾向性检查可能适合未成年人。我们以遗传性黑色素瘤为例,来说明成年癌症向儿童人群遗传风险交流的基本原理和潜在应用,在儿童人群中,儿童期行为可能会降低其晚年罹患疾病的风险。我们从成人黑素瘤的遗传风险交流和儿科健康行为变化文献中吸取经验,以建议可以向患有遗传性黑素瘤风险的儿童及其家庭提供基因检测报告和补充教育的方法,以促进儿童参与预防黑素瘤行为。遗传发现将继续提供新的机会,以向包括儿童在内的未受影响的个体提供易感性遗传风险信息,并可在提供个性化和转化性癌症预防方法的计划中提供。

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