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One test that can be performed when balance is affected is a videonystagmography. The test checks for eye movements that can't be controlled, which is a sign of balance issues.
An optical coherence tomography (OCT) may also be performed. This noninvasive imaging test uses light waves to take a picture of the retina.
There are an array of hearing aids available. These may be a good choice for those with type 2 or 3 Usher syndrome, who start to develop hearing problems later in life.
Eyeglasses can be prescribed at any stage of the syndrome. Other vision aids may also be recommended (e.g. magnifiers, etc.).
Fundus autofluorescence (FAF) imaging is also an option when it comes to diagnosis tools. Blue light is used to take a picture of the retina.
Usher syndrome is a genetic condition that primarily manifests in children. The inherited disorder can affect vision, hearing, and balance. Depending on the specific type of Usher syndrome, symptoms can appear in newborns or only later in life.
In this gallery, we look at the causes, symptoms, and treatments available for those born with Usher syndrome. Click on for more.
Diagnosis will depend on the symptoms. For instance, if a child is born with hearing problems, then hearing tests will be conducted. Genetic testing may also be done to rule out Usher syndrome or other conditions.
Usher syndrome doesn't have a cure. Early intervention services may be offered to children born with the syndrome, while others will benefit from management of symptoms throughout their lifetime.
Sources: (Cleveland Clinic) (Usher Syndrome Coalition) (National Center on Deaf-Blindness)
See also: Genetic mutations that increase vulnerability to certain disorders
Vision tests can also be prescribed. These often include tests for retinitis pigmentosa. An electroretinography (ERG) may be performed to check how the retina responds to light.
As mentioned previously, both parents must carry Usher syndrome genes, meaning that these are inherited in an autosomal recessive pattern.
If the mutation is only present in one of the parents, then the child will carry the gene that causes Usher syndrome but most likely won’t have any symptoms.
A child has a one in four chance of having Usher syndrome if the genetic mutation is present in both biological parents.
Usher syndrome is a rare condition. It’s estimated that it affects between three and six out of every 100,000 people. According to the Usher Syndrome Coalition, there are about 400,000 people who have Usher syndrome worldwide.
Balance issues may manifest when the child starts to walk. Trouble sitting up is also often reported in those with type 1 Usher syndrome.
Vision loss is progressive and usually starts with loss of night vision by around age 10. Vision loss becomes more severe as the person grows older.
Balance is not affected in those with type 3 Usher syndrome. As for vision and hearing problems, they are not present from birth and tend to develop in late childhood, progressively getting worse.
Those with type 1 are born with hearing loss. Babies may be born with profound hearing loss or complete deafness.
Depending on the affected genes, and their combination, hearing, vision, and balance are affected in different ways at different ages. Let’s take a look at the most common types.
Children may find it difficult to move around in the dark. They may also take longer to adjust to changes in lighting, as well as not seeing or even tripping over objects.
Vision loss is also a symptom of Usher syndrome. This is caused by a condition called retinitis pigmentosa (RP).
As an inherited condition, the genetic mutations are passed on through DNA. For the syndrome to occur, both parents must carry one or more mutated genes.
Usher syndrome is a genetic disorder that can affect vision, hearing, and balance. The syndrome was named after Scottish ophthalmologist Charles Usher in 1914.
Those with type 2 Usher syndrome are born with hearing loss, but don’t experience balance issues. Vision problems tend to develop gradually during adolescence and evolve to severe vision loss later in life.
Vision loss tends to be progressive, starting with difficulty in seeing in low light, progressing to tunnel vision (loss of peripheral vision), and potentially then progressing into blindness.
Balance affects those with a specific type of Usher syndrome, often present from birth. Not every person with the syndrome experiences balance issues though.
One of the main symptoms of Usher syndrome is hearing loss. This tends to be quite severe; some babies are even born completely deaf.
There are at least 10 known gene mutations that can lead to the syndrome. These mutations then affect people in different ways.
Cochlear implants are good options for babies born with hearing loss. These small electronic devices can really make a difference.
Understanding Usher syndrome
The condition mostly manifests during childhood
HEALTH Genetic disorder
Usher syndrome is a genetic condition that primarily manifests in children. The inherited disorder can affect vision, hearing, and balance. Depending on the specific type of Usher syndrome, symptoms can appear in newborns or only later in life.
In this gallery, we look at the causes, symptoms, and treatments available for those born with Usher syndrome. Click on for more.