Spina Bifida Research Could Help Treat Eye Defects


New research into Spina Bifida could lead to new treatment for eye defects and eye diseases, experts claim. Researchers at the University of Leeds have newly identified a birth defect gene linked to the condition that is known to cause birth defects and abnormalities including eye problems. It is hoped that the research could lead to the development of further research into and treatments for eye conditions including strabismus.

Spina Bifida is one of the most common permanently disabling birth defects. The condition occurs when the spine does not properly develop in the womb and is though to affect 1 in every 1000 children. Children with Spina Bifida are prone to developing hydrocephalus - the blockage of a ventricle in the brain that causes a build up of cerebrospinal fluid that raises pressure levels in the brain. Hydrocephalus can cause a range of vision problems including cerebral visual impairment, visual field loss, nystagmus, strabismus and more.

Researchers at the University of Leeds studied DNA donated by people with spina bifida and were able to discover a new gene that mutates and impairs cell communication in the womb. Researchers hope to further study the gene to gain further insight into the development of Spina Bifida and various related problems, including vision impairment, that can be caused by the condition.

30th May 2010

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