SNAI2 Gene Waardenburg Syndrome Type 2D NGS Genetic DNA Test
The SNAI2 Gene Waardenburg Syndrome Type 2D NGS Genetic DNA Test is an advanced genetic test designed to identify mutations in the SNAI2 gene, which are associated with Waardenburg syndrome type 2D. This condition is characterized by hearing loss, changes in pigmentation, and various neurological disorders. Understanding your genetic makeup is crucial for early diagnosis and management of these conditions.
What the Test Measures
This test specifically detects mutations in the SNAI2 gene, allowing healthcare providers to assess the risk of developing Waardenburg syndrome type 2D and related neurological disorders.
Who Should Consider This Test?
Individuals with:
- A family history of Waardenburg syndrome or related neurological disorders.
- Symptoms such as hearing loss, changes in skin or hair pigmentation.
- Concerns about genetic predisposition to neurological conditions.
Benefits of Taking the Test
- Provides clarity on genetic risks associated with Waardenburg syndrome.
- Guides healthcare decisions and management strategies.
- Offers peace of mind through understanding one’s genetic health.
Understanding Your Results
Your test results will indicate whether mutations in the SNAI2 gene are present. A genetic counseling session is recommended to help interpret these results and discuss potential implications for you and your family.
Test Pricing
Discount Price | Regular Price |
---|---|
40,000 KSh | 56,000 KSh |
We have branches across Kenya, providing convenient access to our services. Additionally, we offer home sample collection for your convenience.
Book Your Test Today!
Don’t wait to understand your genetic health. Contact us at +254711564616 to book your SNAI2 Gene Waardenburg Syndrome Type 2D NGS Genetic DNA Test today!
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card. Please ensure to provide a clinical history of the patient and consider a genetic counseling session to draw a pedigree chart of affected family members.