100,000 English newborns to be screened for 200 genetic disorders using whole genome sequencing.

The NHS in England is launching a pioneering initiative to screen 100,000 newborns for over 200 genetic disorders using whole genome sequencing. This program aims to enhance early diagnosis and treatment, potentially transforming outcomes for affected infants. Blood samples from umbilical cords will be analyzed to identify conditions that can be treated before symptoms arise. The pilot, set to expand to 40 hospitals, represents a significant advancement in newborn healthcare.

October 02, 2024
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