Summary
- The NHS in England will analyze the genetic code of up to 100,000 newborn babies to diagnose over 200 rare diseases.
- Blood samples will be taken from umbilical cords to identify gene disorders like haemophilia and spinal muscular atrophy.
- Screening involves sequencing the complete DNA of newborns to detect treatable conditions that develop early in childhood.
- The study aims to provide early diagnosis and treatment for genetic diseases, potentially saving lives.