HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test
Introduction
The HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test is a specialized diagnostic test designed to identify mutations in the HOXA1 gene, which are associated with brainstem dysgenesis. This condition can lead to significant developmental challenges, and early detection is vital for managing symptoms and planning treatment.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the HOXA1 gene. It detects specific mutations that may contribute to brainstem dysgenesis, providing crucial information for affected individuals and their families.
Who Should Consider This Test?
Individuals with a family history of brainstem dysgenesis or related symptoms should consider this test. Symptoms may include developmental delays, issues with coordination, and other neurological concerns. Additionally, those with a clinical history suggesting potential genetic conditions should consult their healthcare provider regarding testing.
Benefits of Taking the Test
- Early identification of genetic conditions.
- Informed family planning and management strategies.
- Access to targeted therapies and interventions.
- Genetic counseling for affected families.
Understanding Your Results
Results from the HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test will be provided with a comprehensive report. It’s essential to discuss these results with a healthcare professional, as they will help interpret the implications for the patient and family members.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across all major cities in Kenya, providing convenient access to our services. To book the HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test or for more information, please call or WhatsApp us at +254711564616.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The test requires a sample type of blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to gather the clinical history of the patient and to draw a pedigree chart of affected family members.
