Usher syndrome is a rare inherited disorder primarily characterized by deafness due to an impaired ability of the auditory nerves to transmit sensory input to the brain (sensorineual hearing loss) accompanied by retinitis pigmentosa, a disorder that causes progressive loss of vision.

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A-Z Deafblindness
An in-depth article by Mary Guest, Head of Usher Services at Sense. Includes a detailed description of Usher syndrome, the symptoms, genetics, transmission, associated problems and what can be done.
Boys Town National Research Hospital: Usher Syndrome
Provides information on types 1, 2 and 3 of this condition, retinitis pigmentosa, hearing loss, balance, gene studies, and other conditions which may have similar symptoms.
National Institutes of Health: Usher Syndrome
Provides information including a description of the condition, resources, how to join a NIH clinical study, and funding opportunities for researchers studying the condition.
NIDCD: Usher Syndrome
Factsheet on this condition that affects both hearing and vision, its causes, characteristics and treatment.
Patient: Usher Syndrome
Provides information on this genetic defect causing retinitis pigmentosa and congenital deafness and often vestibular dysfunction. Includes classification, presentation, differential diagnosis and management.
Losing your sight as a deaf person
The BBC reports on deaf people who then become blind. (June 15, 2015)
Deaf woman’s shock as she hears for first time
The BBC reports on a video of the moment a 39-year-old woman heard for the first time, thanks to cochlear implants. (March 28, 2014)
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September 25, 2015 at 17:49:42 UTC
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