Usher syndrome is related to 3 to 6 percent of all childhood deafness and about 50% of deaf-blindness in adults, representing about half of all people who are both deaf and blind. The syndrome is caused by genetic mutations causing retinitis pigmentosa and congenital deafness.
Get the full picture. We’ve designed the robust and cost-effective Usher Panel to help you understand the cause of hearing deficit and blindness in Usher syndrome. Otogenetics Usher Gene Panel has been used to identify gene mutations and copy number variation (CNV) in the Usher genes. In addition, clinical researchers used Otogenetics Usher Gene Panel Testing to investigate Usher gene mutation frequency in certain population.
The Otogenetics Usher Gene Testing assesses 10 genes known to be related to usher syndrome in a single test.
The genetic causes for many Usher syndrome patients remain unknown. Novel genetic causes for Usher may be identified by a more comprehensive genetic test. Want to examine more genes for the diagnosis of novel genetic causes of rare diseases including Usher syndrome? Click here to view our clinical whole exome sequencing.
Otogenetics Usher Gene Testing can be used for clinical diagnostic of patients. For clinical diagnosis, click the requisition form link on the right to download the Requisition Form for the testing.
Otogenetics Usher Gene Testing can also be used for
research, which will not require a clinical report, but raw sequencing data or
selected analysis options. For researchers interested at Otogenetics Usher
Panel, click to submit a quote request for more information.
Download the Test Requisition Here