Nx Gen Sequencing Usher Syndrome Test
The Nx Gen Sequencing Usher Syndrome Test is a comprehensive genetic test designed to identify mutations associated with Usher Syndrome, a genetic disorder that leads to hearing loss and progressive vision impairment. Understanding your genetic predisposition is crucial for early intervention and management of this condition.
What the Test Measures
This test analyzes specific genes known to be involved in Usher Syndrome, including:
- CDH23
- CIB2
- CLRN1
- DFNB31
- ADGRV1
- MYO7A
- PCDH15
- PDZD7
- USH1C
- USH1G
- USH2A
By detecting mutations in these genes, the test provides insights into the risk of developing Usher Syndrome.
Who Should Consider This Test
This test is recommended for individuals experiencing:
- Hearing loss
- Vision impairment
- Family history of Usher Syndrome
- Symptoms suggestive of genetic hearing and vision disorders
Benefits of Taking the Test
Taking the Nx Gen Sequencing Usher Syndrome Test offers several advantages:
- Early diagnosis allows for timely intervention and management.
- Informed family planning decisions can be made.
- Access to support resources and treatment options tailored to specific genetic findings.
- Understanding the genetic basis of the condition can aid in monitoring and managing symptoms.
Understanding Your Results
Results from this test will provide information about the presence of specific genetic mutations. A healthcare professional will help interpret the results and discuss the implications for your health and potential treatment options.
Test Pricing
Test Name | Discount Price (KSh) | Regular Price (KSh) |
---|---|---|
Nx Gen Sequencing Usher Syndrome Test | 57,330 | 63,700 |
How to Book Your Test
We have branches across all major cities in Kenya, offering convenience and accessibility for your testing needs. To book the Nx Gen Sequencing Usher Syndrome Test, please call or WhatsApp us at +254711564616. We also provide home sample collection services for your convenience.
Pre-Test Instructions
Before the test, it is essential to complete the Whole Exome Sequencing Consent Form (Form 37). Please ensure that you submit 10 mL (5 mL min.) of whole blood from 2 Lavender Top (EDTA) tubes, shipped refrigerated. DO NOT FREEZE.
The turnaround time for results is typically 45 working days from the day samples are received.
Take charge of your health today with the Nx Gen Sequencing Usher Syndrome Test!