ATXN7 Gene Spinocerebellar Ataxia Type 7 Autosomal Dominant NGS Genetic DNA Test
The ATXN7 Gene Spinocerebellar Ataxia Type 7 Autosomal Dominant NGS Genetic DNA Test is a vital diagnostic tool for individuals suspected of having hereditary ataxia. This test utilizes Next Generation Sequencing (NGS) technology to identify mutations in the ATXN7 gene, which is associated with Spinocerebellar Ataxia Type 7 (SCA7), a progressive neurological disorder.
Importance of the Test
Understanding your genetic makeup is essential for early diagnosis and management of neurological disorders. The ATXN7 gene plays a crucial role in the development of SCA7, and this test can provide clarity about the risk of developing this condition, allowing for timely intervention and planning.
What the Test Measures
This genetic test detects mutations in the ATXN7 gene, which are responsible for the autosomal dominant inheritance of Spinocerebellar Ataxia Type 7. By analyzing a blood sample or extracted DNA, healthcare professionals can determine if a patient carries the gene mutation.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Those with a family history of Spinocerebellar Ataxia or other neurological disorders.
- Patients exhibiting symptoms such as balance problems, coordination difficulties, or muscle weakness.
- Individuals seeking genetic counseling for family planning.
Benefits of Taking the Test
The benefits of the ATXN7 Gene Spinocerebellar Ataxia Type 7 test include:
- Early diagnosis and understanding of potential health risks.
- Informed decision-making regarding lifestyle and treatment options.
- Access to genetic counseling and support for affected families.
Understanding Your Results
Results from the ATXN7 test will indicate whether a mutation is present. A positive result may suggest a higher risk of developing SCA7, while a negative result may provide reassurance. It is important to discuss results with a healthcare provider or genetic counselor for proper interpretation and guidance.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
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 SCA7.
Book Your Test Today
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu. For a comprehensive understanding of your genetic health, book the ATXN7 Gene Spinocerebellar Ataxia Type 7 Autosomal Dominant NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616.
