HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test
Introduction
The HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test is an advanced genetic test designed to identify mutations in the HOXA1 gene, which are linked to Athabaskan brainstem dysgenesis syndrome. This syndrome is characterized by significant neurological deficits, including developmental delays and difficulties in communication. Understanding genetic predispositions is crucial for early diagnosis and intervention.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect specific mutations in the HOXA1 gene. By analyzing the genetic material, healthcare providers can ascertain whether an individual carries the genetic markers associated with this syndrome.
Who Should Consider This Test?
This test is recommended for:
- Individuals with a family history of Athabaskan brainstem dysgenesis syndrome.
- Patients exhibiting symptoms such as developmental delays, speech difficulties, or other neurological impairments.
- Families seeking genetic counseling to understand their risks and options.
Benefits of Taking the Test
Understanding your genetic makeup can provide numerous benefits:
- Early diagnosis and intervention strategies.
- Informed family planning decisions.
- Access to specialized healthcare resources and support.
- Peace of mind through understanding of genetic risks.
Understanding Your Results
Upon completion of the test, results will be provided with guidance on interpretation. It is essential to consult with a genetic counselor or healthcare provider to fully understand the implications of your results and the next steps you may need to take.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To book the HOXA1 Gene Athabaskan Brainstem Dysgenesis Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with any inquiries and guide you through the booking process.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the HOXA1 gene.
