The plan outlines the creation of a ‘Genomics Population Health Service’ and the implementation of universal newborn genomic testing and polygenic risk scoring. These tools aim to enable early identification and intervention for individuals at high risk of developing common diseases, which implicitly includes cancers.
It is one of the aims of this campaign that there should be specific screening available for those exposed to DES.
The UK National Screening Committee (UK NSC) which advises the Government on screening programmes, has never been asked to consider the evidence for screening people exposed to DES in utero. We can use this commitment to ‘early identification and intervention for individuals at high risk’ to support our call for screening.
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