A woman from Bath hoping to become the first deafblind person to climb Mount Everest has said she is aware of how hard the ...
NEW YORK - Scientists have identified a gene mutation associated with one form of Usher syndrome -- an inherited disorder in which children are born deaf and later lose their sight. The discovery may ...
Usher Syndrome type 1F is a rare but severe genetic disease that causes deafness, lack of balance, and progressive blindness. Now, a team led by researchers at Harvard Medical School, Massachusetts ...
When Rosalyn and Justin Porcano’s daughter Lia was born in 2018, they quickly realized something wasn’t quite right. Within the first 12 hours following her birth, Lia had failed her newborn hearing ...
Steven McCoy, the first recognized black deafblind journalist in the US, and Rebecca Alexander, an award-winning author and psychotherapist who is almost completely blind and deaf will take the stage ...
Researchers have grown 'mini eyes', which make it possible to study and better understand the development of blindness in a rare genetic disease called Usher syndrome for the first time. Researchers ...
ORLANDO, Florida -- Those with Usher Syndrome -- the leading hereditary cause for simultaneous deafness and blindness, for which there is no treatment -- may have a new reason for hope now that ...
SAN RAFAEL -- Two Bay Area parents have created a global organization that is raising funds to research a genetic disorder that robs children of their sight and hearing. Marin couple Rosalyn and ...
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