Abstract
This chapter aims to explore the multitude of challenges that limit the clinician’s ability to rapidly identify cancer predisposition syndromes in children with cancer. The current clinical approaches as well as novel strategies for CPS screening and detection will also be discussed. In particular, the integration of comprehensive germline sequencing and the development of eHealth technologies in pediatric oncology practice will be presented in this chapter.
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Reichman, L., Goudie, C. (2021). Recognition of Cancer Predisposition Syndromes. In: Malkin, D. (eds) The Hereditary Basis of Childhood Cancer. Springer, Cham. https://doi.org/10.1007/978-3-030-74448-9_16
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DOI: https://doi.org/10.1007/978-3-030-74448-9_16
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