Usher syndrome is a rare, inherited disorder that involves loss of hearing and sight.
is due to the inability of the auditory nerves to send sensory input to the brain. This is called sensorineural hearing loss.
The vision loss, called
(RP), usually happens after age 10. RP is a deterioration of the retina. The retina is a layer of light-sensitive tissue that lines the back of the eye. It changes visual images into nerve impulses in the brain that allow us to see.
RP slowly gets worse over time.
Nerve and Retina of the Eye
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Three types of Usher syndrome have been identified: types I, II, and III. The age of onset and severity of symptoms separate the different types.
Usher syndrome is caused by a genetic mutation. A child must inherit one defective gene from each parent in order to develop Usher syndrome. A child with one defective gene is a carrier and will not have any symptoms. It is not clear what causes the mutation in the gene.
The only known factor that increases the risk of Usher syndrome is having parents with the disorder and/or parents who carry the genes for the disorder. If both parents carry the abnormal gene, a child has a 25% chance of inheriting both of these abnormal genes and developing Usher syndrome.
The main symptoms of Usher syndrome are hearing and vision loss. Psychological or behavioral disorders may occur before vision loss. Some people also have balance problems due to inner ear problems.
RP limits a person’s ability to see in dim light or the dark. It also causes a person to lose side vision slowly over time. Eventually, any vision that is left is only in a small, tunnel-shaped area. Almost everyone with RP becomes legally blind. There is no way of knowing when or how quickly a person will lose vision.
Symptoms and characteristics of each type include the following: Type I Deaf at birth and receives little or no benefit from hearing aidsSevere balance problemsSlow to sit without supportRarely learn to walk before age 18 monthsRP begins by age 10 with difficulty seeing at night, and quickly changes to blindnessType II Born with moderate to severe hearing loss, and can benefit from hearing aidsNo balance problemsRP begins in the teenage yearsType III Born with normal hearing that gets worse in the teenage years and leads to deafness by mid to late adulthoodBorn with near-normal balanceRP begins in the early teenage years as difficulty seeing at night, and leads to blindness by mid-adulthood
The doctor will ask about your symptoms and medical history. A physical exam will be done. Hearing loss is determined with standard hearing tests. Balance problems can be detected with a test called electronystagmography (ENG). In this test, the doctor flushes the ears with warm and then cool water. This causes nystagmus, which is rapid eye movements that can help the doctor detect a balance disorder.
An eye doctor will perform an eye exam, which will likely include the following: Visual field test to check side visionTest to check for ability to adapt to seeing in the darkTest to check sensitivity to color and contrast
If any problems are found on these tests, an electroretinography (ERG) is done. This test confirms a diagnosis of RP. It measures the electricity given off by the nerves in the retina. The test is done while wearing special contact lenses and looking at a flashing light.
There is no cure for Usher syndrome. The best treatment is to identify the disorder as early as possible and begin educational programs and services right away. This helps reduce the communication and learning problems that can result from hearing and vision loss.
The specific programs and services depend on the severity of the hearing, vision, and balance problems, and the person's age and abilities. Options include: Hearing aidsAssistive listening devicesCochlear implant—a small device surgically put under the skin behind the ear to give deaf people some ability to hear
Adjustment and career counselingTraining to help with balance and movementLow vision servicesCommunications trainingSkills in living independently
Other potential treatments are being investigated. Talk to your doctor about the risks and benefits of participating in a clinical trial.
There are no current guidelines to prevent Usher syndrome.
Dammeyer J. Children with Usher syndrome: Mental and behavioral disorders.
Behav Brain Funct. 2012;8:16.
Lopes VS, Williams DS. Gene therapy for the retinal degeneration of Usher syndrome caused by MYO7A. Cold Spring Harb Perspect Med. 2015;5(6).
Usher syndrome. Boys Town National Research Hospital website. Available at:
http://www.boystownhospital.org/research/molecularstudies/pages/ushersyndrome.aspx. Accessed February 12, 2016.
Usher syndrome? Foundation Fighting Blindness website. Available at:
http://www.blindness.org/eye-conditions/usher-syndrome. Accessed February 12, 2016.
Usher syndrome. National Institute on Deafness and Other Communication Disorders website. Available at:
www.nidcd.nih.gov/health/hearing/pages/usher.aspx. Updated April 30, 2014. Accessed February 12, 2016.
Last reviewed February 2016 by Rimas Lukas, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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