26/02/2026
🧬Genomic study helps detect baby’s rare growth condition
Doctors at Cambridge University Hospitals NHS Foundation Trust are “thrilled” by a baby’s positive response to treatment after her rare genetic condition was diagnosed following results from a national screening study.
"With the help of the Generation Study we have a clear genetic diagnosis for Safi. It has made it much easier for us to identify the right treatment and to get her started on it sooner. If all goes well, her life should be unaffected by her condition." said Dr Emile Hendriks, Consultant Paediatric Endocrinologist at CUH.
Read more on the CUH website: https://www.cuh.nhs.uk/news/genomic-study-detect-rare-growth-condition/
Register your interest in taking part: https://www.generationstudy.co.uk/