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How three-parent babies could be key to beating mitochondrial disease

Pioneering research in the UK could stop genetic defects in newborns – but the treatment is contentious

United kingdomUnited statesDarren griffinFrances flinterDame kayDame kay daviesNuffield council on bioethicsOxford universityUniversity of kentEmbryology authorityUniversity college londonNewcastle fertility centreNewcastle fertilityHuman fertilityProf frances flinterNuffield council

Our son didn t have the energy to walk or talk, but now I can t keep up with him

Genome sequencing and early detection could change the lives of children with rare health conditions, but the implications may prove testing

United kingdomWest yorkshireUnited kingdom generalCity ofRichard scottRob everittFrances flinterDepartment of healthNewborns genome programmeNuffield bioethics councilGenomic englandSocial careGenomics englandGreat ormond street hospitalHealth and fitnessChildren 39s health

Babies will get blood tests to see if they have rare childhood cancers

Experts say it has the potential to help 3,000 children a year in England if rolled out, helping many young patients before symptoms appear.

United kingdomDame sally daviesSteve barclayStephen powisDavid cameronFrances flinterCancer research unitedCancer research united kingdomDepartment of healthNewborn genomes programmeEngland nationalSocial careDaily mailBeat childrenPrime minister david cameronHuman genome project

New £105m scheme aims to speed up diagnosis of rare genetic diseases in newborns

‘We want to be able to offer speedy diagnosis, quicker access to treatment, and better outcomes and quality of life,’ Dr Rich Scott said.

United kingdomSteve barclay james manningSteve barclayFrances flinterNewborn genomes programmeDepartment of health social careGenomics englandSocial careRich scottSecretary steve barclayProfessor frances flinterEmeritus professorClinical geneticsHealth secretary steve barclayGenomics england led

Genome sequencing trial to test benefits of identifying genetic diseases at birth

Study with 100,000 babies to look at faster diagnosis of rare conditions and how genetic data might be used

United kingdomRichard scottSarah norcrossFrances flinterProgress educational trustGenomics england

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