HEXA Gene TaySachs Disease NGS Genetic DNA Test
Introduction
The HEXA Gene TaySachs Disease NGS Genetic DNA Test is a vital diagnostic tool designed to identify mutations in the HEXA gene, which are responsible for Tay-Sachs disease, a severe genetic disorder that affects the nervous system. This test employs Next Generation Sequencing (NGS) technology, allowing for a comprehensive analysis of the genetic material.
Importance of the Test
Understanding your genetic predisposition to Tay-Sachs disease is essential, especially for individuals with a family history of the condition. Early detection can lead to better management strategies and informed reproductive choices, ultimately improving quality of life.
What the Test Measures
This test specifically detects mutations in the HEXA gene. It provides insights into whether an individual is a carrier of Tay-Sachs disease or if they are affected by it.
Who Should Consider This Test?
- Individuals with a family history of Tay-Sachs disease.
- People of Ashkenazi Jewish descent, as they are at a higher risk.
- Those experiencing symptoms of metabolic disorders.
Benefits of Taking the Test
- Identifies carriers of the HEXA gene mutation.
- Informs family planning and reproductive decisions.
- Provides peace of mind for individuals with a family history of the disease.
- Enables early intervention and management strategies.
Understanding Your Results
Results will indicate whether you carry the HEXA gene mutation. A positive result may suggest that you are a carrier or affected by Tay-Sachs disease, while a negative result indicates that no mutations were found. It is essential to discuss your results with a healthcare provider or genetic counselor for further guidance.
Test Details
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| HEXA Gene TaySachs Disease NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the HEXA Gene TaySachs Disease NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Ensure you have a clinical history and consider a genetic counseling session to discuss family history related to Tay-Sachs disease.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can include blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a genetic counseling session is recommended to draw a pedigree chart of family members affected by Tay-Sachs disease.
Consult with a general physician or a genetics specialist for more information about this essential test.
