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Retinitis Pigmentosa-Deafness Syndrome
An Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that is caused by mutation in the MTTS2 gene in the mitochondrial genome.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
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Overview
Usher syndrome is an inherited disease that causes serious hearing loss and retinitis pigmentosa, an eye disorder that causes your vision to get worse over time. It is the most common condition that affects both hearing and vision. There are three types of Usher syndrome: People with type I are deaf from birth and have severe balance problems from a young age. Vision problems usually start by age 10 and lead to blindness. People with type II have moderate to severe hearing loss and normal balance. Vision problems start in the early teens and get worse more slowly than in type I. People with type III are born with normal hearing and near-normal balance but develop vision problems and then…
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.