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Usher Syndrome |
Deafness-retinitis pigmentosa syndrome; dystrophia retinae pigmentosa-dysostosis syndrome; Graefe-Usher syndrome; Hallgren syndrome; Retinitis pigmentosa-deafness syndrome |
Usher syndrome is a genetic disease causing deaf-blindness. It is essentially progressive retinitis pigmentosa combined with congenital hearing impairment. It is inherited in an autosomal recessive pattern and is estimated to occur in 1 in 10,000 people. While this is a rare genetic condition, it represents the major cause of syndromic deafness with blindness. The condition gets its name from British ophthalmologist, C.H. Usher, who in 1914 wrote a paper describing several cases in which the ...
Wikipedia - [full article]
Usher Syndrome Articles
- Usher Syndrome
... Usher syndrome is the most common condition that involves both hearing and vision problems. A syndrome is a disease or disorder that has more than one feature or symptom. The major symptoms of Usher s... - Usher syndrome
... Usher syndrome is characterized by hearing loss or deafness and progressive vision loss due to retinitis pigmentosa (RP). RP is a condition that affects the retina (the part of the eye that detects li... - Usher Syndrome: New Insights Lead to Earlier Treatment
... Children with an inherited hearing and vision disorder known as Usher syndrome can now benefit from better treatment options, thanks to a recent scientific discovery of a method to identify this disor...
Resources
- Cómo Hablarle a su Oculista (National Eye Institute)
- Diagram of the Eye (National Eye Institute)
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