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Yorkshire Eye Research Mission statement Yorkshire Eye Research was launched in 2000 as the northern branch of the National Eye...+ Full Story |
Case studies Case study: Leber's congenital amaurosisLeber’s congenital amaurosis (LCA) is a rare...+ Full Story | Other Articles | ||
| Glaucoma Discovery |
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| Written by Administrator |
| Monday, 04 January 2010 13:09 |
| Dr Manir Ali (University of Leeds) has identified a mutation of the LTBP2 gene as the cause of Primary Congenital Glaucoma, a devastating condition which affects over 6,000 people in the UK. It is hoped that this discovery will aid medical professionals in screening for the disease, as early diagnosis and swift treatment is vital in slowing its prognosis. |
| Last Updated on Monday, 04 January 2010 13:14 |
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