Usher syndrome
What are the symptoms?
There are three types of the syndrome. Type I is characterised by profound congenital hearing loss, poor balance and retinitis pigmentosa before the age of 10. Type II presents moderate to severe hearing loss, normal balance and retinitis pigmentosa develops in the late teens or early 20's. Type III is characterised by progressive hearing loss and Retinitis Pigmentosa progressing at a variable rate, generally with onset around the second or third decade of life.
Background
| How is it diagnosed? ![]()