Research team makes important step toward a therapy for a rare genetic disease
Usher Syndrome type 1F is a rare but severe genetic disease that causes deafness, lack of balance, and progressive blindness.
Apr 26, 2023
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Usher Syndrome type 1F is a rare but severe genetic disease that causes deafness, lack of balance, and progressive blindness.
Apr 26, 2023
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In the spiraling cycle that can lead to vision loss in premature newborns, Medical College of Georgia scientists have found a new target and drug that together appear to stop the destruction in its tracks.
Apr 20, 2023
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Researchers at Case Western Reserve University and the Cleveland Clinic in Cleveland, Ohio, have investigated the potential link between new-onset retinal vascular occlusion (RVO) after receiving the COVID-19 vaccination ...
Usher syndrome, a rare inherited genetic disease, is a leading cause of combined deafness and blindness with type 2A (USH2A) being the most common form. USH2A, caused by mutations in the USH2A gene, can include hearing loss ...
Apr 17, 2023
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Social determinants of health (SDOH), across multiple domains, are associated with vision loss, according to a study published online April 6 in JAMA Ophthalmology.
Apr 11, 2023
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Early detection of childhood hearing loss is crucial but also challenging because babies can't tell their parents or doctors exactly what's wrong.
Mar 27, 2023
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Indiana University School of Medicine researchers have identified a new therapeutic target that could lead to more effective treatment of glaucoma.
Mar 10, 2023
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An outbreak of serious bacterial infections in 13 U.S. states linked to use of artificial tears has prompted experts to offer tips for keeping dry eyes safe.
Mar 6, 2023
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Using Burt's Bees to get buzzed? Bad idea.
Mar 2, 2023
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An international panel led by a pediatric neuroimmune expert and co-director of the Neuroscience Center at Children's Hospital of Philadelphia (CHOP) has established new criteria for properly diagnosing myelin oligodendrocyte ...
Feb 16, 2023
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