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- £28 Million boost to understand child health
- The impact of sex selection and abortion in China, India and South Korea
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- New Policy Research Unit in the Health of Children, Young People and Families
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- ICH Open Day 2011
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- Tate Liverpool exhibition inspires pioneering science games
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- Great Ormond Street Hospital Children’s Charity announces plans to build a Centre for Children’s Rare Disease Research
- Gene therapy shows clinical effect in third immune disease
- Clean delivery kits linked to substantial reduction in neonatal deaths in South Asia, study shows
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- Research reveals association between red hair gene and rare birthmarks
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- Professor of economics and deputy director appointed to the new UK Birth Cohort Study
- First example of a heritable abnormality affecting semantic cognition found
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- ICH OPEN DAY AND POSTER COMPETITION
- Europe’s first research centre to battle birth defects
- New cause of thyroid hormone deficiency discovered
- £10 million boost for Centre for Children’s Rare Disease Research
- EU awards grant to develop new drug for Duchenne muscular dystrophy
- New research centre for teenagers with arthritis
- Major study shows steep decline in figure for diagnosed epilepsy
- Obesity leads to vitamin D deficiency
- Researchers find gene responsible for rare condition that can lead to melanomas
- ICH research highlights unmet needs of children and young people with cancer and challenges public policy
- Amniotic fluid stem cells repair gut damage
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- Overall child deaths due to injuries are down in the UK
- Aug 13
- Prestigious NIHR Research Professorship awarded to Professor Persis Amrolia
£10 million boost for Centre for Children’s Rare Disease Research
26 November 2012
A centre bringing together the country’s leading clinicians and researchers to find effective treatments for children’s rare diseases has received a £10 million funding boost.
The Centre for Children’s Rare Disease Research will bring together expertise from Great Ormond Street Hospital and University College London, in particular the UCL Institute of Child Health, to advance understanding and find treatments for children’s rare diseases.
The £10 million award from the Higher Education Funding Council for England (HEFCE) is a significant step towards raising the £85 million needed to build and equip the Centre. Great Ormond Street Hospital Children’s Charity has undertaken to raise the remaining amount and the HEFCE funding was given as part of a governmental initiative to support projects which have private funding from industry or the charitable sector worth a minimum of double the public contribution.
Professor David Goldblatt is Director of Clinical Research and Innovation for Great Ormond Street Hospital and the UCL Institute of Child Health and an academic lead for the new Centre. He said: “This is fantastic news. The Centre will provide huge opportunities to advance research into children’s rare diseases and translate discoveries into effective treatment quicker than ever before."
“The work will not simply assist in finding treatments for rare diseases but will inform our understanding of generic and more common disease mechanisms.”
The new Centre, to be built adjacent to Great Ormond Street Hospital and the UCL Institute of Child Health, will work to find treatments and cures for rare diseases, of which there are 6,000 identified. Seventy five per cent of rare diseases affect children. These include rare cancers such as childhood cancers, and some other better known conditions such as cystic fibrosis and muscular dystrophy.
Central to the work of the researchers and clinicians working in the new facility will be finding ways to speed up the delivery of effective treatments, as 30 per cent of children with rare diseases will not live past their fifth birthday.
Great Ormond Street Hospital is uniquely placed to advance research to tackle these life-threatening and life limiting conditions, as it sees many more children with rare disease than any other hospital in the country and is already working with researchers from ICH, many of whom are also clinicians, on ground breaking research in this area.
Current rare disease research
includes work looking at the molecular basis of rare cancers,
ciliopathies and rare obesity syndromes as well as novel genetic
therapies for diverse conditions including inherited muscular
dystrophies and rare immune deficiencies.
For further information, please contact Jenny Gimpel at the GOSH-ICH Press Office on 020 7239 3178, firstname.lastname@example.org.
For genuine and urgent out-of-hours queries call switchboard on 020 7405 9200.
Page last modified on 26 nov 12 11:44