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CRISPR used to repair blindness-causing genetic defect in patient-derived stem cells

Researchers used CRISPR to repair a genetic mutation responsible for retinitis pigmentosa, an inherited condition causing blindness in at least 1.5 million cases worldwide. The study marks the first time researchers have replaced a defective gene associated with a sensory disease in stem cells derived from a patient's tissue.

SourceColumbia University Irving Medical Center·JournalScientific Reports·DateJan 27, 2016

Teaching the blind to draw -- and do STEM

E.A.S.Y. LLC has received a $1 million NIH grant to develop an interactive graphics printer that translates conventional graphics to raised-line versions for the blind, enabling them to take math and science courses like sighted students. The printer will be used in schools nationwide to create accessible worksheets.

Seeing sound

Researchers discovered that intrinsic neural connections can be used to help the blind detect their environment, making tasks easier and more intuitive. The study used a sensory substitution device to translate images into sound, allowing blind people to associate different sounds with features of their environment.

SourceCalifornia Institute of Technology·JournalScientific Reports·DateOct 26, 2015

We've all got a blind spot, but it can be shrunk

Scientists have found that training can effectively reduce the size of the human blind spot, improving vision in individuals with age-related macular degeneration. The researchers trained participants on a direction-discrimination task for 20 consecutive weekdays, resulting in a 10% reduction in functional blindness.

SourceCell Press·JournalCurrent Biology·DateAug 31, 2015

Finding hope in the dark

Researchers have identified a gene, PRDM8, linked to early loss of night vision in animal models. Gene therapy for Leber's congenital amaurosis shows promising results, but temporary improvements are seen.

SourceUniversity of Bristol·JournalProceedings of the National Academy of Sciences·DateJun 10, 2015

New form of inherited blindness discovered

Researchers found that DRAM2 gene mutations lead to loss of central vision and peripheral vision loss in older individuals, likely due to reduced autophagy and photoreceptor renewal. The discovery sheds new light on the condition and highlights the importance of collaboration between institutions.

SourceUniversity of Leeds·JournalAmerican Journal of Human Genetics·DateMay 14, 2015

Study shows new technology may improve management of leading causes of blindness

A new non-invasive OCT technology has been developed that can improve the clinical management of macular degeneration, diabetic eye disease and glaucoma, the leading causes of blindness in the United States. The technology allows for earlier diagnosis and treatment, enabling more timely intervention to prevent irreversible loss of vision.

SourceOregon Health & Science University·JournalProceedings of the National Academy of Sciences·DateApr 20, 2015

New pathways discovered to prevent blindness

Scientists at Monash University have made a major breakthrough in understanding how the brain adapts to vision loss by discovering a second pathway for visual information. This new pathway, through the pulvinar area of the brain, plays a crucial role in rerouting visual information following injury or trauma.

SourceMonash University·JournalCurrent Biology·DateFeb 16, 2015

Most prescription labels fail to meet guidelines, risking dosage errors

A recent study by the University of Waterloo found that most prescription labels in Canada do not follow recommended guidelines for legibility. The researchers suggest that improving label appearance can be achieved without new technologies or larger labels, and recommends a patient-centered approach to labelling standards.

SourceUniversity of Waterloo·JournalCanadian Pharmacists Journal / Revue des Pharmaciens du Canada·DateJul 9, 2014